Skip to main content
American Journal of Human Genetics logoLink to American Journal of Human Genetics
. 1957 Dec;9(4):331–349.

Bibliography of Human Genetics

Richard H Post
PMCID: PMC1932022  PMID: 13498002

Full text

PDF
331

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. AGUSTSSON M. H., LIPSCOMB P. R., MILLS S. D., SOULE E. H. Aettgeng neurofibromatosis hjá barni med rhabdomyosarcoma og neurofibrosarcoma. Laeknabladid. 1955;39(8-9):113–123. [PubMed] [Google Scholar]
  2. ALAJOUANINE T., SCHERRER J., CONTAMIN F., MARTEAU R., CALVET J. A propos de l'association dyssynergia cerebellaris myoclonica de R. Hunt et hérédo-dégénération spino-cérébelleuse type Friedreich; etude clinique et électromyographique d'un cas. Rev Neurol (Paris) 1955;93(3):577–581. [PubMed] [Google Scholar]
  3. ALBERT-CREMIEUX, DONGIER M. Observations statistiques sur les familles où survient une anorexie mentale. Ann Med Psychol (Paris) 1956 Apr;114(4):639–641. [PubMed] [Google Scholar]
  4. ALLARD R. A propos de la conservation génétique du sickle cell trait. Ann Soc Belg Med Trop (1920) 1955 Dec 31;35(6):649–660. [PubMed] [Google Scholar]
  5. ALLEN G., BAROFF G. S. Mongoloid twins and their siblings. Acta Genet Stat Med. 1955;5(4):294–326. doi: 10.1159/000150779. [DOI] [PubMed] [Google Scholar]
  6. ALLISON A. C. Sickle-cell anaemia and haemoglobin C. Trans R Soc Trop Med Hyg. 1956 May;50(3):185-96; discussion, 197-203. doi: 10.1016/0035-9203(56)90023-2. [DOI] [PubMed] [Google Scholar]
  7. ALLISON A. C. The sickle-cell and haemoglobin C genes in some African populations. Ann Hum Genet. 1956 Jul;21(1):67–89. [PubMed] [Google Scholar]
  8. ANASTASI A. Intelligence and family size. Psychol Bull. 1956 May;53(3):187–209. doi: 10.1037/h0047353. [DOI] [PubMed] [Google Scholar]
  9. ANGELINI C. Osservazioni di tre casi di paralisi spinale spastica familiare. Riv Neurol. 1956 Mar-Apr;26(2):225–230. [PubMed] [Google Scholar]
  10. ARDOUIN Le fibro-geodisme bimandibulaire héréditaire et la displasie fibreuse des os. Rev Laryngol Otol Rhinol (Bord) 1956 May-Jun;77(5-6):565–591. [PubMed] [Google Scholar]
  11. ARNEAUD J. D., YOUNG O. A preliminary survey of the distribution of A B O and Rh blood groups in Trinidad, B.W.I. Doc Med Geogr Trop. 1955 Dec;7(4):375–378. [PubMed] [Google Scholar]
  12. AUERBACH C. A possible case of delayed mutation in man. Ann Hum Genet. 1956 May;20(4):266–269. doi: 10.1111/j.1469-1809.1955.tb01281.x. [DOI] [PubMed] [Google Scholar]
  13. AVERILL J. H. Wolff-Parkinson-White syndrome occurring in brothers. Am Heart J. 1956 Jun;51(6):943–945. doi: 10.1016/0002-8703(56)90237-x. [DOI] [PubMed] [Google Scholar]
  14. AVERY M. E. Hereditary elliptocytosis and hemoglobin C trait; a report of two cases. Bull Johns Hopkins Hosp. 1956 Mar;98(3):184–196. [PubMed] [Google Scholar]
  15. AVOGARO P. Le ipoconvertinemie congenite e familiari; rassegna sinottica della letteratura e presentazione di un caso di osservazione personale sensibile alla vitamin K. Acta Med Patav. 1956 Jan-Mar;16(1):1–40. [PubMed] [Google Scholar]
  16. BACKHAUSZ R., NEMESKERI J. Résultats des recherches séro-anthropologiques effectuées au Bodrogköz (Hongrie Nord-Est). J Genet Hum. 1955 Dec;4(4):219–233. [PubMed] [Google Scholar]
  17. BARNICOT N. A. The relation of the pigment trichosiderin to hair colour. Ann Hum Genet. 1956 Jul;21(1):31–39. doi: 10.1111/j.1469-1809.1971.tb00263.x. [DOI] [PubMed] [Google Scholar]
  18. BARRAQUER-BORDAS L., BARRAQUER-FERRE L., ROVIRA M. Etude clinique et radiologique d'une acropathie ulcéromutilante familiale. Acta Neurol Psychiatr Belg. 1955 Dec;55(12):978–983. [PubMed] [Google Scholar]
  19. BARRETO A. D., ALBERTO M. S. Estudos antropológicos dos povos Bantos; contribuiço para o estudo dos grupos sanguíneos dos indigenas Moçambicanos. An Inst Med Trop (Lisb) 1953 Dec;10(4 Pt 2):3569–3594. [PubMed] [Google Scholar]
  20. BECKER W. Uber einen Fall familiärer Osteopoikile (Albers-Schönberg). Medizinische. 1956 Apr 7;(14):526–527. [PubMed] [Google Scholar]
  21. BEDFORD P. D., JAMES F. E. A family with the progressive hypertrophic polyneuritis of Dejerine and Sottas. J Neurol Neurosurg Psychiatry. 1956 Feb;19(1):46–51. doi: 10.1136/jnnp.19.1.46. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. BENDELAC, BENZAQUEN, LEVYLEBHAR J. P. Eventration diaphragmatique d'origine congénitale et familiale. Maroc Med. 1955 Sep;34(364):1112–1113. [PubMed] [Google Scholar]
  23. BENNETT J. H., WALKER C. B. Fertility and blood groups of some East Anglian blood donors. Ann Hum Genet. 1956 May;20(4):299–308. doi: 10.1111/j.1469-1809.1955.tb01284.x. [DOI] [PubMed] [Google Scholar]
  24. BERGLIN C. G. On the concepts and calculus of penetrance. Acta Genet Stat Med. 1955;5(3):240–262. doi: 10.1159/000150773. [DOI] [PubMed] [Google Scholar]
  25. BERNHEIM M., BERGER M., UZAN R. Le rôle des facteurs génétiques dans le développement du myxoedème congénital. C R Seances Soc Biol Fil. 1955 Aug-Sep;149(15-18):1553–1558. [PubMed] [Google Scholar]
  26. BIMBI-KOVACS A. E., HARDYMENT A. F. Potter's facies associated with polycystic kidney, with Laurence-Biedl-Moon syndrome in siblings. Can Med Assoc J. 1956 Apr 1;74(7):549–551. [PMC free article] [PubMed] [Google Scholar]
  27. BIRAN S. Die dynamische und die genetische Erklärung der Neurose. Acta Psychother Psychosom Orthopaedagog. 1956;4(1):1–20. [PubMed] [Google Scholar]
  28. BLAUSTEIN A. Treatment of thrombosis occurring in individuals with hereditary hemorrhagic telangiectasis; report of three cases including two members of one family. Angiology. 1956 Feb;7(1):55–60. doi: 10.1177/000331975600700107. [DOI] [PubMed] [Google Scholar]
  29. BLOCK W. D., RUKAVINA J. G., CURTIS A. C. Serum electrophoretic studies on patients with familial primary systemic amyloidosis. J Lab Clin Med. 1956 Mar;47(3):357–364. [PubMed] [Google Scholar]
  30. BOOK J. A., FRACCARO M. Genetical investigations in a North-Swedish population; mandibulo-facial dysostosis. Acta Genet Stat Med. 1955;5(4):327–333. doi: 10.1159/000150780. [DOI] [PubMed] [Google Scholar]
  31. BOOK J. A., KOSTMANN R. Prospects of biochemical genetics in medicine. Ann Hum Genet. 1956 Feb;20(3):251–252. doi: 10.1111/j.1469-1809.1956.tb01370.x. [DOI] [PubMed] [Google Scholar]
  32. BORKENHAGEN R., VAZIRANI S. Multiple neurofibromatosis in a family. Oral Surg Oral Med Oral Pathol. 1956 Mar;9(3):269–274. doi: 10.1016/0030-4220(56)90004-4. [DOI] [PubMed] [Google Scholar]
  33. BOYD W. C. The accuracy of estimates of MNS gene frequences. Acta Genet Med Gemellol (Roma) 1956 May;5(2):234–237. doi: 10.1017/s1120962300020618. [DOI] [PubMed] [Google Scholar]
  34. BOYD W. C. The inheritance of the blood groups. Am J Clin Pathol. 1956 Jun;26(6):654–657. doi: 10.1093/ajcp/26.6.654. [DOI] [PubMed] [Google Scholar]
  35. BRAIN P. The sickle-cell phenomenon. Cent Afr J Med. 1956 Feb;2(2):73–77. [PubMed] [Google Scholar]
  36. BRANDT W. Uber familiäre neuro-vaskuläre Dystrophie; ulzerierende Akropathie. Z Orthop Ihre Grenzgeb. 1956;87(3):489–492. [PubMed] [Google Scholar]
  37. BRIHAYE M., NENQUIN-KLAASSEN E., BERTHOLET G. Atrophie musculaire neurogène du type Charcot-Marie-Tooth-Hoffman, associée à une atrophie optique bilatérale. Acta Neurol Psychiatr Belg. 1956 May;56(5):302–312. [PubMed] [Google Scholar]
  38. BROSH R. Zur Frage des nicht-hämolytischen familiären Icterus. Helv Paediatr Acta. 1956 May;11(2):172–178. [PubMed] [Google Scholar]
  39. BUCKWALTER J. A., WOHLWEND E. B., COLTER D. C., TIDRICK R. T. Natural selection associated with the ABO blood group. Science. 1956 May 11;123(3202):840–841. doi: 10.1126/science.123.3202.840-a. [DOI] [PubMed] [Google Scholar]
  40. BUNGE R. G., BRADBURY J. T. Genetic sex: chromatin test versus gonadal histology. J Clin Endocrinol Metab. 1956 Aug;16(8):1117–1119. doi: 10.1210/jcem-16-8-1117. [DOI] [PubMed] [Google Scholar]
  41. CABANNES R., SENDRA L., DALAUT Hemoglobinose D; anomalie hémoglobinique héréditaire retrouvée chez l'Algérien Musulman; observations de deux familles. Alger Medicale. 1955 Jun;59(6):387–395. [PubMed] [Google Scholar]
  42. CAFIERO F., CAZZANIGA G. Osservazioni sulla tubercolosi polmonare nei nuclei familiari; genitori e figli, germani. G Ital Della Tuberc. 1956 May-Jun;10(3):139–145. [PubMed] [Google Scholar]
  43. CAMPBELL C. J., PEDRA G. Sternomastoid tumor in identical twins. J Bone Joint Surg Am. 1956 Apr;38-A(2):350–352. [PubMed] [Google Scholar]
  44. CAMPBELL M., TURNER-WARWICK M. Two more families with cardiomegaly. Br Heart J. 1956 Jul;18(3):393–402. doi: 10.1136/hrt.18.3.393. [DOI] [PMC free article] [PubMed] [Google Scholar]
  45. CANNON J. F. Diabetes insipidus; clinical and experimental studies with consideration of genetic relationships. AMA Arch Intern Med. 1955 Aug;96(2):215–272. doi: 10.1001/archinte.1955.00250130089012. [DOI] [PubMed] [Google Scholar]
  46. CARPITELLA A. L'ereditarietà psicopatica. II. Oligofrenia gemellare. Rass Neuropsichiatr. 1955 May-Jun;9(3):159–171. [PubMed] [Google Scholar]
  47. CARPITELLA A. L'ereditarietà psicopatica. III. Microcefalia familiare. Rass Neuropsichiatr. 1955 May-Jun;9(3):172–180. [PubMed] [Google Scholar]
  48. CARROLL F. D. Hereditary afections. Trans Am Acad Ophthalmol Otolaryngol. 1956 Jan-Feb;60(1):58–59. [PubMed] [Google Scholar]
  49. CARTEAUD A., MAMOU H. Sur 2 cas de xanthomatoses; hyperlipémie essentielle et xanthomatose familiale; action de l'héparine locale. Sem Hop. 1956 Apr 30;32(26):1501–1504. [PubMed] [Google Scholar]
  50. CASESA P. R. Familial leptocytosis. N Y State J Med. 1956 May 15;56(10):1631–1639. [PubMed] [Google Scholar]
  51. CASTELLO R. Il fattore Rh nell'eziologia della sordità. Arch Sci Med (Torino) 1955 Dec;100(6):530–536. [PubMed] [Google Scholar]
  52. CEPPELLINI R., SINISCALCO M. Una nuova ipotesi genetica per il sistema Lewis secretore e suoi riflessi nei riguardi di alcune evidenze di linkage con altri loci. Riv Ist Sieroter Ital. 1955 Nov-Dec;30(6):431–445. [PubMed] [Google Scholar]
  53. CHANDLER J. H., BEBIN J. Hereditary cerebellar ataxia; olivopontocerebellar type. Neurology. 1956 Mar;6(3):187–195. doi: 10.1212/wnl.6.3.187. [DOI] [PubMed] [Google Scholar]
  54. CHAUDHURI R. N., SAHA T. K., BASU S. P., MUKHERJEE A. M., CHAUDHURI M. N. R. Chronic splenomegaly. Indian J Med Res. 1956 Apr;44(2):305–323. [PubMed] [Google Scholar]
  55. CHEESEMAN E. A., CROZIER C. M., MERRETT J. D. Data on linkage in man: hereditary deafness in Northern Ireland. Ann Hum Genet. 1956 Jul;21(1):59–66. doi: 10.1111/j.1469-1809.1971.tb00265.x. [DOI] [PubMed] [Google Scholar]
  56. CLEMETSON C. A. The difference in birth weight of human twins. Twin blood studies. III. Placental transfer of amino-acids. J Obstet Gynaecol Br Emp. 1956 Feb;63(1):15–18. doi: 10.1111/j.1471-0528.1956.tb05429.x. [DOI] [PubMed] [Google Scholar]
  57. COCHRANE W. A., PAYNE W. W., SIMPKISS M. J., WOOLF L. I. Familial hypoglycemia precipitated by amino acids. J Clin Invest. 1956 Apr;35(4):411–422. doi: 10.1172/JCI103292. [DOI] [PMC free article] [PubMed] [Google Scholar]
  58. COHEN B. H., GLASS B. The ABO blood groups and the sex ratio. Hum Biol. 1956 Feb;28(1):20–42. [PubMed] [Google Scholar]
  59. COLBOURNE M. J., EDINGTON G. M. Sickling and malaria in the Gold Coast. Br Med J. 1956 Apr 7;1(4970):784–786. doi: 10.1136/bmj.1.4970.784. [DOI] [PMC free article] [PubMed] [Google Scholar]
  60. COLLIER W. A. The M-N blood-groups in the Arawaks of Matta, Surinam. Doc Med Geogr Trop. 1955 Dec;7(4):359–360. [PubMed] [Google Scholar]
  61. COLLINS D. H. Paget's disease of bone; incidence and subclinical forms. Lancet. 1956 Jul 14;271(6933):51–57. doi: 10.1016/s0140-6736(56)90422-6. [DOI] [PubMed] [Google Scholar]
  62. COX M. J. Progressive familial hypertrophic polyneuritis (Dejerine-Sottas Syndrome, 1893). Proc R Soc Med. 1956 Apr;49(4):183–184. doi: 10.1177/003591575604900406. [DOI] [PMC free article] [PubMed] [Google Scholar]
  63. CROME L., KIRMAN B. H., MARRS M. Rhesus incompatibility and mental deficiency. Brain. 1955;78(4):514–536. doi: 10.1093/brain/78.4.514. [DOI] [PubMed] [Google Scholar]
  64. CUTBUSH M., GIBLETT E. R., MOLLISON P. L. Demonstration of the phenotype Le (a+ B+) in infants and in adults. Br J Haematol. 1956 Apr;2(2):210–220. doi: 10.1111/j.1365-2141.1956.tb06829.x. [DOI] [PubMed] [Google Scholar]
  65. DA SILVA A. X. Contribuiço para o estudo antropológico de Goa pelos grupos sanguíneos. An Inst Med Trop (Lisb) 1953 Dec;10(4 Pt 2):3557–3568. [PubMed] [Google Scholar]
  66. DAH' N. L., ODEGARD J. On hereditary factors in functional psychoses; preliminary report on a research project in two Norwegian mental hospitals. Acta Psychiatr Neurol Scand Suppl. 1956;106:320–335. [PubMed] [Google Scholar]
  67. DAS S. R. A contribution to the heredity of the P.T.C. taste character based on a study of 845 sib-pairs. Ann Hum Genet. 1956 May;20(4):334–343. doi: 10.1111/j.1469-1809.1955.tb01288.x. [DOI] [PubMed] [Google Scholar]
  68. DAVIDSON S., WATSON C. W. Hereditary light sensitive epilepsy. Neurology. 1956 Apr;6(4):235–261. doi: 10.1212/wnl.6.4.235. [DOI] [PubMed] [Google Scholar]
  69. DE ANDRADE FILHO O. Moléstia de Milroy. J Pediatr (Rio J) 1955 Oct;20(10):586–593. [PubMed] [Google Scholar]
  70. DE VAAL O. M. Genital intersexuality in three brothers, connected with consanguineous marriages in the three previous generations. Acta Paediatr. 1955 Jan;44(1):35–39. doi: 10.1111/j.1651-2227.1955.tb04110.x. [DOI] [PubMed] [Google Scholar]
  71. DEBUSK A. G. Metabolic aspects of chemical genetics. Adv Enzymol Relat Subj Biochem. 1956;17:393–476. doi: 10.1002/9780470122624.ch9. [DOI] [PubMed] [Google Scholar]
  72. DEFOREST R. E. Four cases of benign left bundle branch block in the same family. Am Heart J. 1956 Mar;51(3):398–404. doi: 10.1016/0002-8703(56)90065-5. [DOI] [PubMed] [Google Scholar]
  73. DELAGE J. M. Pancytopénie familiale. Laval Med. 1956 Mar;21(3):334–350. [PubMed] [Google Scholar]
  74. DELAY J., BRION S., BADARACCO J. C. Le diagnostic différentiel des maladies de Pick et d' Alzheimer; a propos de 12 observations anatomo-cliniques. Encephale. 1955;44(5):454–499. [PubMed] [Google Scholar]
  75. DEMIRAG B., ERTAT S. A propos d'une famille de myxoedémateux. Ann Paediatr. 1956 Feb;186(2):83–86. [PubMed] [Google Scholar]
  76. DENT C. E., HARRIS H. Hereditary forms of rickets and osteomalacia. J Bone Joint Surg Br. 1956 Feb;38-B(1):204–226. doi: 10.1302/0301-620X.38B1.204. [DOI] [PubMed] [Google Scholar]
  77. DERIAN P. S. Coxa plana in dizygotic male twins. J Bone Joint Surg Am. 1956 Jul;38-A(4):901–907. [PubMed] [Google Scholar]
  78. DESCAMPS L., VAN BOGAERT L. Documents anatomocliniques sur les idioties amaurotiques. I. Sur une forme infantile précoce isolée dans une souche aryenne. J Genet Hum. 1956 Apr;5(1):54–72. [PubMed] [Google Scholar]
  79. DEUCHAR D. C. Werner's syndrome. Proc R Soc Med. 1956 Jun;49(6):316–317. [PubMed] [Google Scholar]
  80. DI SANT'AGNESE P. A. Fibrocystic disease of the pancreas, a generalized disease of exocrine glands. J Am Med Assoc. 1956 Mar 10;160(10):846–853. doi: 10.1001/jama.1956.02960450028007. [DOI] [PubMed] [Google Scholar]
  81. DICKINS A. M., RICHARDSON J. R., PIKE L. A., ROBERTS J. A. F. Further observations on ABO blood-group frequencies and toxaemia of pregnancy. Br Med J. 1956 Apr 7;1(4970):776–777. doi: 10.1136/bmj.1.4970.776. [DOI] [PMC free article] [PubMed] [Google Scholar]
  82. DIEKE W. Beobachtung eines Falles von familiärem Pseudohermaphroditismus masculinus mit Ausbildung sekundärer weiblicher Geschlechtsmerkmale. Zentralbl Gynakol. 1956 Jun 9;78(23):916–927. [PubMed] [Google Scholar]
  83. DORN H. Dominanter Erbgang beim Epithelioma adenoides cysticum Brooke. Z Haut Geschlechtskr. 1956 Jan 15;20(2):43–46. [PubMed] [Google Scholar]
  84. DU PAN R. M., PACCAUD M. Etude des anticorps antipoliomyélitiques dans certaines families de Genève. Ann Paediatr. 1956 Feb;186(2):120–121. [PubMed] [Google Scholar]
  85. DURAND P., PRIMON G., GARIBIZZO S. Osservazioni sull'eredità della galattosemia. Pediatr Prat. 1956 May;27(5):147–152. [PubMed] [Google Scholar]
  86. EBBING H. C. Uber Diabetes insipidus, insbesondere seine erblichen Formen. Z Mensch Vererb Konstitutionsl. 1956;33(5):415–424. [PubMed] [Google Scholar]
  87. EDINGTON G. M., LEHMANN H. The sickle-cell gene. Am J Clin Pathol. 1956 May;26(5):553–555. [PubMed] [Google Scholar]
  88. EILANDER J. M. Albinisme in een Papoea-gemeenschap. Ned Tijdschr Geneeskd. 1956 Feb 11;100(6):399–402. [PubMed] [Google Scholar]
  89. ELLBORG A., FORSSMAN H. Nephrogenic diabetes insipidus in children. Acta Paediatr. 1955 May;44(3):209–218. doi: 10.1111/j.1651-2227.1955.tb04134.x. [DOI] [PubMed] [Google Scholar]
  90. ELPHINSTONE R. H., WICKES I. G., ANDERSON A. B. Familial agamma-globulinaemia. Br Med J. 1956 Aug 11;2(4988):336–338. doi: 10.1136/bmj.2.4988.336. [DOI] [PMC free article] [PubMed] [Google Scholar]
  91. ENG L. I. L., MURSADIK, LIOE L. D., ODANG U. Haemoglobin E-thalassaemia disease in Indonesia. Doc Med Geogr Trop. 1956 Jun;8(2):135–143. [PubMed] [Google Scholar]
  92. ERLANDSON M., SMITH C. H., SCHULMAN I. Thalassemia-hemoglobin C disease in white siblings. Pediatrics. 1956 May;17(5):740–746. [PubMed] [Google Scholar]
  93. ESSEN-MOLLER E. The calculation of morbid risk in parents of index cases, as applied to a family sample of schizophrenics. Acta Genet Stat Med. 1955;5(4):334–342. doi: 10.1159/000150781. [DOI] [PubMed] [Google Scholar]
  94. EVANS R. L. Red-cell survival in familial haemolytic anaemias. Nature. 1956 May 5;177(4514):839–840. doi: 10.1038/177839a0. [DOI] [PubMed] [Google Scholar]
  95. FANTL P., SAWERS R. J. Occurrence of different prothromboplastin deficiencies in related male bleeders. Br J Haematol. 1956 Jan;2(1):102–105. doi: 10.1111/j.1365-2141.1956.tb06691.x. [DOI] [PubMed] [Google Scholar]
  96. FEDERICI P. C. La pressione arteriosa nei soggetti sani normali. III. Influenza dell'ereditarietà sui valori pressori di soggetti sani con genitori ipertesi. Arch Patol Clin Med. 1955;32(3):178–191. [PubMed] [Google Scholar]
  97. FENDEL H. Eine toxoplasmotische Zwillingsgeburt. Virchows Arch Pathol Anat Physiol Klin Med. 1955;327(3):293–303. doi: 10.1007/BF00955744. [DOI] [PubMed] [Google Scholar]
  98. FISCHER S. Primary perivascular cerebral, cerebellar and leptomeningeal melanoma; congenital aphasia and familial predisposition to naevi verrucosi. Acta Psychiatr Neurol Scand. 1956;31(1):21–34. doi: 10.1111/j.1600-0447.1956.tb04718.x. [DOI] [PubMed] [Google Scholar]
  99. FISHER S., MENDELL D. The communication of neurotic patterns over two and three generations. Psychiatry. 1956 Feb;19(1):41–46. doi: 10.1080/00332747.1956.11023030. [DOI] [PubMed] [Google Scholar]
  100. FORSSMAN H. Is hereditary diabetes insipidus of nephrogenic type associated with mental deficiency? Acta Psychiatr Neurol Scand. 1955;30(4):577–587. doi: 10.1111/j.1600-0447.1955.tb01010.x. [DOI] [PubMed] [Google Scholar]
  101. FORSTER W., TYNDEL M. The neuropsychiatric aspects of familial dysautonomia (the Riley-Day syndrome). J Ment Sci. 1956 Apr;102(427):345–348. doi: 10.1192/bjp.102.427.345. [DOI] [PubMed] [Google Scholar]
  102. FRANCESCHETTI A. Manifestation de blépharochalasis chez le père, associé à des doubles lèvres apparaissant également chez sa fillette âgée d'un mois. J Genet Hum. 1955 Sep;4(3):181–184. [PubMed] [Google Scholar]
  103. FRANCOIS J. La recherche des conducteurs de gènes en pathologie oculaire. Bull Acad R Med Belg. 1955;20(6):228–249. [PubMed] [Google Scholar]
  104. FRANCOIS J., VERRIEST G., DE ROUCK A. L'achromatopsie congenitale. Doc Ophthalmol. 1955;9(2):338–424. [PubMed] [Google Scholar]
  105. FRANCOIS J., VERRIEST G., DE ROUCK A. La maladie d'Oguchi. Ophthalmologica. 1956 Jan;131(1):1–40. doi: 10.1159/000302795. [DOI] [PubMed] [Google Scholar]
  106. FRASER F. C. Thoughts on the etiology of clefts of the palate and lip. Acta Genet Stat Med. 1955;5(4):358–369. doi: 10.1159/000150783. [DOI] [PubMed] [Google Scholar]
  107. FREUND J. Typen vegetativer Regulationsstörungen im Kindesalter. Z Mensch Vererb Konstitutionsl. 1956;33(4):365–375. [PubMed] [Google Scholar]
  108. FURUHATA T., HASEBE H. Q blood type. Rev Belg Pathol Med Exp. 1955 Oct;24(6):541–549. [PubMed] [Google Scholar]
  109. GALLASCH E. H. Kritische Betrachtungen über die beiden Vererbungstheorien der Rh-Untergruppen. Med Monatsschr. 1955 Nov;9(11):727–730. [PubMed] [Google Scholar]
  110. GALLIARD H., DESCHIENS R., FLOCH H., LITALIEN F. Etude comparée du test de Thorn à l' A. C. T. H. chez des sujets de race mélanoderme et de race leucoderme. Bull Soc Pathol Exot Filiales. 1955;48(3):377–384. [PubMed] [Google Scholar]
  111. GAMSTORP I. Adynamia episodica hereditaria. Acta Paediatr Suppl. 1956 May;45(Suppl 108):1–126. [PubMed] [Google Scholar]
  112. GARNER L. L., GROSSMANN E. E. Hereditary hemorrhagic telangiectass; with beta irradiation of a conjunctival lesion. Am J Ophthalmol. 1956 Apr;41(4):672–679. [PubMed] [Google Scholar]
  113. GATTO I., ALBEGGIANI A. Panmielopatia costituzionale con malformazioni multiple (sindrome di Fanconi). Acta Genet Med Gemellol (Roma) 1956 May;5(2):190–212. [PubMed] [Google Scholar]
  114. GAUNT R. T., LECUTIER M. A. Familial cardiomegaly. Br Heart J. 1956 Apr;18(2):251–258. doi: 10.1136/hrt.18.2.251. [DOI] [PMC free article] [PubMed] [Google Scholar]
  115. GEDDA L. Little's syndrome of familial type; two couples of DZ discordant twins of the same sibship. Acta Genet Stat Med. 1955;5(4):370–376. doi: 10.1159/000150784. [DOI] [PubMed] [Google Scholar]
  116. GENTILI C., ZAMBONELLI F. Malattia eredo-degenerativa del sistema cerebellare; presentazione di uno stipite familiare. Riv Sper Freniatr Med Leg Alien Ment. 1956 Jun 30;80(1-2):187–206. [PubMed] [Google Scholar]
  117. GIANFERRARI L., ARRIGONI G., CRESSERI A., LOVATI G., MORGANTI G. Ricerche genetiche e clinico-statistiche sulle neoplasie della prostata. Acta Genet Med Gemellol (Roma) 1956 May;5(2):224–233. [PubMed] [Google Scholar]
  118. GIBSON R. Familial idiopathic methaemoglobinaemia associated with oligophrenia. Am J Ment Defic. 1956 Jul;61(1):207–209. [PubMed] [Google Scholar]
  119. GIBSON R. Friedreich's ataxia with initial oligophrenia in siblings. Am J Ment Defic. 1956 Apr;60(4):776–778. [PubMed] [Google Scholar]
  120. GIRAUD P., BERNARD R., ORSINI A., MAESTRAGGI P., THOLANCE A. Degénérescence hépato-lenticulaire chez deux jumeaux. Sem Hop. 1956 Jul 10;32(42-43/6):2441–2443. [PubMed] [Google Scholar]
  121. GLASS B. Blood groups in physical anthropology. Science. 1956 May 25;123(3204):927–928. doi: 10.1126/science.123.3204.927. [DOI] [PubMed] [Google Scholar]
  122. GOMEZ MARTINEZ I., MORON RUBIO J. M. Psicosis sincronicas y homocronas. Rev Clin Esp. 1956 May 15;61(3):159–166. [PubMed] [Google Scholar]
  123. GOSLICH H. Klinische und elektro-retinographische Untersuchungen in drei Generationen von familiär-hereditärer juveniler Makula-Degeneration (Stargardt). Klin Monbl Augenheilkd Augenarztl Fortbild. 1955;127(6):657–663. [PubMed] [Google Scholar]
  124. GOUTTAS A., FESSAS P., TSEVRENIS H., XEFTERI E. Description d'une nouvelle variété d'anémie hémolytique congénitale; etude hématologique, électrophorétique et génétique. Sang. 1955;26(9):911–919. [PubMed] [Google Scholar]
  125. GOYAL R. K., SHARMA B. C., ANAND B. R. Retinoblastoma in Rajasthan. J Indian Med Assoc. 1956 Feb 1;26(3):97–98. [PubMed] [Google Scholar]
  126. GRACE E. J. Genetics, cancer of the lung, and tobacco. Med Times. 1956 Aug;84(8):787–790. [PubMed] [Google Scholar]
  127. GREBE H. Uber besondere Zwillingskonkordanzen. Acta Genet Med Gemellol (Roma) 1956 May;5(2):138–154. [PubMed] [Google Scholar]
  128. GREENBURG W. Hereditary callosities. J Natl Assoc Chirop. 1956 May;46(5):327–328. [PubMed] [Google Scholar]
  129. GREPPI E. L'eredità nel diabete degli adulti con speciale riguardo alle tendenze multiple in varia associazione clinico-metabolica. Riforma Med. 1956 Mar 17;70(11):287–288. [PubMed] [Google Scholar]
  130. GRUPPER C., DAVID J. Lupus érythémateux familial chez la mère et chez le fils. Bull Soc Fr Dermatol Syphiligr. 1955 Nov-Dec;(5):492–493. [PubMed] [Google Scholar]
  131. GUEST G. M. Twins and diabetes mellitus. Diabetes. 1956 Mar-Apr;5(2):150–151. doi: 10.2337/diab.5.2.150. [DOI] [PubMed] [Google Scholar]
  132. HABERMANN P., FLECK M. Uber das Rothmund-Syndrom. Z Kinderheilkd. 1955;77(3):306–321. [PubMed] [Google Scholar]
  133. HACKL E. Epidermolysis bullosa hereditaria vom Typ Weber-Cockayne; ein kasuistischer Beitrag mit Stammbaumskizze. Wien Klin Wochenschr. 1956 May 25;68(21):451–452. [PubMed] [Google Scholar]
  134. HAJEK F., ROTH B. Esenciální hereditární tremor (Mironova nemoc). Cesk Neurol. 1956 Mar;19(1):59–63. [PubMed] [Google Scholar]
  135. HALDANE J. B. Mutation in the sex-linked recessive type of muscular dystrophy; a possible sex difference. Ann Hum Genet. 1956 May;20(4):344–347. doi: 10.1111/j.1469-1809.1955.tb01289.x. [DOI] [PubMed] [Google Scholar]
  136. HAMBURGER J., CROSNIER J., LISSAC J., NAFFAH J. Sur un syndrome familial de nephropathie avec surdité. J Urol Medicale Chir. 1956 Mar;62(3):113–124. [PubMed] [Google Scholar]
  137. HAMMON W. M., LUDWIG E. H., SATHER G. E., SCHRACK W. D., Jr A longitudinal study of infection with poliomyelitis viruses in American families on a Philippine military base, during an interepidemic period. Ann N Y Acad Sci. 1955 Sep 27;61(4):979–988. doi: 10.1111/j.1749-6632.1955.tb42556.x. [DOI] [PubMed] [Google Scholar]
  138. HANLON D. G., SELBY J. B., BAYRD E. D. Hereditary leptocytosis (thalassemia minor). J Am Med Assoc. 1956 Jul 21;161(12):1132–1135. doi: 10.1001/jama.1956.02970120014004. [DOI] [PubMed] [Google Scholar]
  139. HANSEN-MELANDER E., KULLANDER S., MELANDER Y. Chromosome analysis of a human ovarian cystocarcinoma in the ascites form. J Natl Cancer Inst. 1956 Apr;16(5):1067–1081. [PubMed] [Google Scholar]
  140. HARRIS H., ROBSON E. B. Variation in homozygous cystinuria. Acta Genet Stat Med. 1955;5(4):381–390. doi: 10.1159/000150786. [DOI] [PubMed] [Google Scholar]
  141. HASAERTS-VAN GEERTRUYDEN Sur la sclérose latérale amyotrophique héréditaire; une deuxieme souche belge. J Genet Hum. 1955 Sep;4(3):152–163. [PubMed] [Google Scholar]
  142. HAUGE M., HARVALD B. Heredity in gout and hyperuricemia. Acta Med Scand. 1955 Nov 10;152(4):247–257. doi: 10.1111/j.0954-6820.1955.tb03485.x. [DOI] [PubMed] [Google Scholar]
  143. HEISTO H. Relasjonen mellom blodtype og ulcus-sykdom. Tidsskr Nor Laegeforen. 1956 Jan 1;76(1):10–13. [PubMed] [Google Scholar]
  144. HELWEG-LARSEN H. F., HAUGE M., SAGILD U. Hereditary transient muscular paralysis in Denmark; genetic aspects of family periodic paralysis and family periodic adynamia. Acta Genet Stat Med. 1955;5(3):263–281. doi: 10.1159/000150774. [DOI] [PubMed] [Google Scholar]
  145. HENDERSON A. B. The abnormal hemoglobins. J Natl Med Assoc. 1956 Jul;48(4):221–229. [PMC free article] [PubMed] [Google Scholar]
  146. HERLITZ G. Hereditary allergic constitution in recurrent catarrh of the upper respiratory tract in children. Int Arch Allergy Appl Immunol. 1956;8(4):221–225. doi: 10.1159/000228288. [DOI] [PubMed] [Google Scholar]
  147. HERLITZ G., REDIN B. The prevalence of cerebral palsy. Acta Paediatr. 1955 Mar;44(2):146–154. doi: 10.1111/j.1651-2227.1955.tb04125.x. [DOI] [PubMed] [Google Scholar]
  148. HERLOFSEN H. B., ODEGARD O. A study of psychotic patients of consanguineous parentage. Acta Genet Stat Med. 1955;5(4):391–402. doi: 10.1159/000150787. [DOI] [PubMed] [Google Scholar]
  149. HERMANN H. Das Grönblad-Strandberg-Syndrom in erbbiologischer Betrachtung. Z Haut Geschlechtskr. 1956 Jun 1;20(11):314–317. [PubMed] [Google Scholar]
  150. HERMANN H. Zur Erbpathologie der Acanthosis nigricans. Z Mensch Vererb Konstitutionsl. 1955;33(3):193–202. [PubMed] [Google Scholar]
  151. HERTZBERG R. Tay-Sachs disease: report of three cases in one family. Med J Aust. 1956 Apr 21;43(16):664–665. [PubMed] [Google Scholar]
  152. HIERONS R. Familial peroneal muscular atrophy and its association with the familial ataxias and tremor and longevity. J Neurol Neurosurg Psychiatry. 1956 May;19(2):155–160. doi: 10.1136/jnnp.19.2.155. [DOI] [PMC free article] [PubMed] [Google Scholar]
  153. HOFFMAN J. Pigmentary retinal lipoid neuronal heredodegeneration (Spielmeyer-Vogt disease); the neuro-ophthalmologic considerations. Am J Ophthalmol. 1956 Jul;42(1):15–21. doi: 10.1016/0002-9394(56)90004-6. [DOI] [PubMed] [Google Scholar]
  154. HOFFMANN D. Kardiovasculäre Erkrankungen beim Strandberg-Grönblad-Syndrom. Z Mensch Vererb Konstitutionsl. 1956;33(5):389–403. [PubMed] [Google Scholar]
  155. HOLT L. B. Corneal dystrophies; three dominant heredity types in Piedmont North Carolina. N C Med J. 1956 May;17(5):225–227. [PubMed] [Google Scholar]
  156. HOLT S. B. Genetics of dermal ridges: parent-child correlations for total finger ridge-count. Ann Hum Genet. 1956 May;20(4):270–281. doi: 10.1111/j.1469-1809.1955.tb01282.x. [DOI] [PubMed] [Google Scholar]
  157. HOUSTON J. C., ZILKHA K. J. Haemochromatosis in a family. Guys Hosp Rep. 1955;104(3):262–267. [PubMed] [Google Scholar]
  158. HOWARD A. The hazards from the increasing use of ionizing radiations. III. An attempt to assess the genetic changes resulting from the irradiation of human populations. Br J Radiol. 1956 May;29(341):270–273. doi: 10.1259/0007-1285-29-341-270. [DOI] [PubMed] [Google Scholar]
  159. HUBNER O., HALLERVORDEN J. Ein Geschwisterpaar mit familiärer infantiler diffuser Sklerose vom Typus Krabbe. Zentralbl Allg Pathol. 1956 Mar 20;94(9-10):461–470. [PubMed] [Google Scholar]
  160. HURSEY R. J., Jr, WITKOP C. J., Jr, MIKLASHEK D., SACKETT L. M. Dentinogenesis imperfecta in a racial isolate with multiple hereditary defects. Oral Surg Oral Med Oral Pathol. 1956 Jun;9(6):641–658. doi: 10.1016/0030-4220(56)90325-5. [DOI] [PubMed] [Google Scholar]
  161. HUTCHISON J. H., MCGIRR E. M. Sporadic non-endemic goitrous cretinism; hereditary transmission. Lancet. 1956 Jun 30;270(6931):1035–1037. doi: 10.1016/s0140-6736(56)90800-5. [DOI] [PubMed] [Google Scholar]
  162. ISTVAN L., JILLY P. Haemophilia B (Christmas-betegség, illetve PTC. hiány) kórképével kapcsolatos tapasztalatok. Orv Hetil. 1956 Jan 29;97(5):133–137. [PubMed] [Google Scholar]
  163. IVERSEN T., BASTRUP-MADSEN P. Congenital familial deficiency of factor V (parahaemophilia) combined with deficiency of antihaemophilic globulin. Br J Haematol. 1956 Jul;2(3):265–275. doi: 10.1111/j.1365-2141.1956.tb06698.x. [DOI] [PubMed] [Google Scholar]
  164. JACOB G. F., LEHMANN H., RAPER A. B. Haemoglobin D in Indians of Gujerati origin in Uganda. East Afr Med J. 1956 Apr;33(4):135–138. [PubMed] [Google Scholar]
  165. JAMESON R. J., LAWLER S. D., RENWICK J. H. Nail-patella syndrome: clinical and linkage data on family G. Ann Hum Genet. 1956 May;20(4):348–360. doi: 10.1111/j.1469-1809.1955.tb01290.x. [DOI] [PubMed] [Google Scholar]
  166. JANSEN L. H. Le mode de transmission de la malade d'Ehlers-Danlos. J Genet Hum. 1955 Dec;4(4):204–218. [PubMed] [Google Scholar]
  167. JENNINGS D., BALME R. H., RICHARDSON J. E. Carcinoma of stomach in relation to ABO blood-groups. Lancet. 1956 Jul 7;271(6932):11–12. doi: 10.1016/s0140-6736(56)91386-1. [DOI] [PubMed] [Google Scholar]
  168. JEQUIER M., DUFOUR R. Résultats d'une enquête médicale et génétique dans une population d'aveugles faibles d'esprit. Bull Schweiz Akad Med Wiss. 1955 Oct;11(4-5):363–378. [PubMed] [Google Scholar]
  169. JOHN G. G., KNUDTSON K. P. Chronic idiopathic jaundice; two cases occurring in siblings, with histochemical studies. Am J Med. 1956 Jul;21(1):138–142. doi: 10.1016/0002-9343(56)90030-4. [DOI] [PubMed] [Google Scholar]
  170. JOKL E. The contribution of twin research to the physiology of exercise. Acta Genet Med Gemellol (Roma) 1956 Jan;5(1):115–122. doi: 10.1017/s1120962300027062. [DOI] [PubMed] [Google Scholar]
  171. JORDAN W. M. Familial tuberous sclerosis. Br Med J. 1956 Jul 21;2(4985):132–135. doi: 10.1136/bmj.2.4985.132. [DOI] [PMC free article] [PubMed] [Google Scholar]
  172. JULIAO O. F., CANELAS H. M., LONGO N. A. Idiotia amaurótica familiar, forma juvenil; estudo clínico e laboratorial de três casos. Arq Neuropsiquiatr. 1956 Jun;14(2):136–157. doi: 10.1590/s0004-282x1956000200003. [DOI] [PubMed] [Google Scholar]
  173. KALLMANN F. J., ROTH B. Genetic aspects of preadolescent schizophrenia. Am J Psychiatry. 1956 Feb;112(8):599–606. doi: 10.1176/ajp.112.8.599. [DOI] [PubMed] [Google Scholar]
  174. KALLMANN F. J. The genetics of aging. J Chronic Dis. 1956 Aug;4(2):140–152. doi: 10.1016/0021-9681(56)90014-5. [DOI] [PubMed] [Google Scholar]
  175. KALMUS H. Genetical responses to season and day. Acta Med Scand Suppl. 1955;307:59–62. doi: 10.1111/j.0954-6820.1955.tb16307.x. [DOI] [PubMed] [Google Scholar]
  176. KAPILA C. C., KAUL S., CHATTERJEE B. C. Glycogen-storage disease of liver. Br Med J. 1956 Apr 21;1(4972):893–897. doi: 10.1136/bmj.1.4972.893. [DOI] [PMC free article] [PubMed] [Google Scholar]
  177. KAPPELER R. Familiäre Hämochromatose; zugleich ein Beitrag zur Frage der Herzinsuffizienz und zur Aderlasstherapie bei Hämochromatose. Schweiz Med Wochenschr. 1956 May 12;86(19):477–481. [PubMed] [Google Scholar]
  178. KAWAMURA T. Uber die Herkunft der Naevuszellen und die genetische Verwandtschaft zwischen Pigmentzellnaevus, blauem Naevus und Recklinghausenscher Phakomatose. Hautarzt. 1956 Jan;7(1):7–14. [PubMed] [Google Scholar]
  179. KAYSER R. Uber infantile familiäre Opticusatrophie. Confin Neurol. 1955;15(5):310–323. [PubMed] [Google Scholar]
  180. KIRCHOFF H., RIGDON R. H. Frequency of cancer in the white and Negro: a study based upon necropsies. South Med J. 1956 Aug;49(8):834–841. doi: 10.1097/00007611-195608000-00009. [DOI] [PubMed] [Google Scholar]
  181. KIRMAN B. H., BLACK J. A., WILKINSON R. H., EVANS P. R. Familial pitressin-resistant diabetes insipidus with mental defect. Arch Dis Child. 1956 Feb;31(155):59–66. doi: 10.1136/adc.31.155.59. [DOI] [PMC free article] [PubMed] [Google Scholar]
  182. KISSEL P., ARNOULD G., HARTEMANN P., DUREUX J., DEBRY G. L'électroencéphalogramme dans la maladie de Friedreich. Rev Neurol (Paris) 1955 Nov;93(5):761–764. [PubMed] [Google Scholar]
  183. KITE J. H. Dwarfs; a discussion of four causative conditions. J Med Assoc Ga. 1956 Mar;45(3):86–88. [PubMed] [Google Scholar]
  184. KLEIN D. Idiotie familiale associée à des troubles somatiques et endocriniens. J Genet Hum. 1955 Dec;4(4):256–258. [PubMed] [Google Scholar]
  185. KLEIN D. Le pronostic génetique dans le diabète. J Genet Hum. 1955 Sep;4(3):185–187. [PubMed] [Google Scholar]
  186. KLEIN D. Maladie fibro-kystique du pancréas. J Genet Hum. 1955 Dec;4(4):259–260. [PubMed] [Google Scholar]
  187. KLEIN S. J. Blood group frequencies tables. J Lab Clin Med. 1956 Jun;47(6):920–922. [PubMed] [Google Scholar]
  188. KNOX W. E. The molecular concept of hereditary diseases. Bull Tufts N Engl Med Cent. 1956 Jan-Mar;2(1):1–8. [PubMed] [Google Scholar]
  189. KOSTMANN R. Infantile genetic agranulocytosis; agranulocytosis infantilis hereditaria. Acta Paediatr Suppl. 1956 Feb;45(Suppl 105):1–78. [PubMed] [Google Scholar]
  190. KROOP I. G. The production of tears in familial dysautonomia; preliminary report. J Pediatr. 1956 Mar;48(3):328–329. doi: 10.1016/s0022-3476(56)80258-8. [DOI] [PubMed] [Google Scholar]
  191. KUGELBERG E., WELANDER L. Heredofamilial juvenile muscular atrophy simulating muscular dystrophy. AMA Arch Neurol Psychiatry. 1956 May;75(5):500–509. doi: 10.1001/archneurpsyc.1956.02330230050005. [DOI] [PubMed] [Google Scholar]
  192. KURLAND L. T. Recherches sur la distribution géographique de la sclérose en plaques et de la sclérose latérale amyotrophique; déductions étiologiques. Acta Neurol Psychiatr Belg. 1956 May;56(5):287–301. [PubMed] [Google Scholar]
  193. LADJIMI R., LAKHOUA M. Erythro-kératodermie palmo-plantaire congénitale et familiale. Tunis Med. 1956 Mar;44(3):233–237. [PubMed] [Google Scholar]
  194. LAFON R., PASSOUANT P., FAURE J. L., MINVIELLE J. Epilepsie et gémellite; étude clinique, electroencephalographique et psychologique de 7 couples de jumeaux univitellins épileptiques. Montp Med. 1956 Jan;49(1):56–75. [PubMed] [Google Scholar]
  195. LAMBERT J., PELLETIER A., PARADIS G. Maladie dégénérative familiale; présentation clinique. Laval Med. 1956 Jun;21(6):777–783. [PubMed] [Google Scholar]
  196. LANDAU J., NELKEN E., DAVIS E. Hereditary haemorrhagic telangiectasia; with retinal and conjunctival lesions. Lancet. 1956 Aug 4;271(6936):230–231. doi: 10.1016/s0140-6736(56)90916-3. [DOI] [PubMed] [Google Scholar]
  197. LANDY M., CEPPELLINI R. Production of O inagglutinability in erythrocytes coated with typhoid Vi and O antigens. Nature. 1955 Dec 31;176(4496):1266–1267. doi: 10.1038/1761266a0. [DOI] [PubMed] [Google Scholar]
  198. LARSON C. A. Incestuous matings among parents of mental defectives. Acta Genet Stat Med. 1955;5(4):420–422. doi: 10.1159/000150789. [DOI] [PubMed] [Google Scholar]
  199. LATERZA A., PAPARO F. Ptosi congenita ereditaria. Riv Neurol. 1956 Jan-Feb;26(1):105–106. [PubMed] [Google Scholar]
  200. LAURENT Y. Le caractère familial de l'ostéochondrose disséquante. J Belge Radiol. 1956;39(1):19–21. [PubMed] [Google Scholar]
  201. LAYRISSE M., ARENDS T. High incidence blood group found in Venezuelan Indians. Science. 1956 Apr 13;123(3198):633–633. doi: 10.1126/science.123.3198.633. [DOI] [PubMed] [Google Scholar]
  202. LAYRISSE M., ARENDS T. The Diego blood factor in Chinese and Japanese. Nature. 1956 Jun 9;177(4519):1083–1084. doi: 10.1038/1771083a0. [DOI] [PubMed] [Google Scholar]
  203. LEHMANN H. A further example of haemoglobin D in a Turkish family. Trans R Soc Trop Med Hyg. 1956 Mar;50(2):178–180. doi: 10.1016/0035-9203(56)90080-3. [DOI] [PubMed] [Google Scholar]
  204. LEHMANN H., RAPER A. B. Maintenance of high sickling rate in an African community. Br Med J. 1956 Aug 11;2(4988):333–336. doi: 10.1136/bmj.2.4988.333. [DOI] [PMC free article] [PubMed] [Google Scholar]
  205. LEHMANN H., RYAN E. The familial incidence of low pseudocholinesterase level. Lancet. 1956 Jul 21;271(6934):124–124. doi: 10.1016/s0140-6736(56)90869-8. [DOI] [PubMed] [Google Scholar]
  206. LEHMANN H., STORY P., THEIN H. Haemoglobin E in Burmese; two cases of haemoglobin E disease. Br Med J. 1956 Mar 10;1(4966):544–547. doi: 10.1136/bmj.1.4966.544. [DOI] [PMC free article] [PubMed] [Google Scholar]
  207. LEIN J. N., STEWART C. T., MOLL F. C. Sex-linked hereditary nystagmus. Pediatrics. 1956 Aug;18(2):214–217. [PubMed] [Google Scholar]
  208. LEVAN A. Chromosomes in cancer tissue. Ann N Y Acad Sci. 1956 Mar 14;63(5):774–792. doi: 10.1111/j.1749-6632.1956.tb50892.x. [DOI] [PubMed] [Google Scholar]
  209. LEVESQUE J., LEPAGE F., BOESWILLWALD M., GRUNER J. Deux cas de dystrophie musculaire familiale congénitale simulant une maladie de Werdnig-Hoffmann-Oppenheim. Arch Fr Pediatr. 1956;13(2):202–207. [PubMed] [Google Scholar]
  210. LEVKOVA N. A. K voprosu o bolezni Shiullera-Kristiana. Pediatriia. 1956 Mar-Apr;39(2):79–80. [PubMed] [Google Scholar]
  211. LILLY H. A. Effect of heart on the "M" antigen of erythrocytes. J Med Lab Technol. 1956 Jan-Apr;13(5-6):401–405. [PubMed] [Google Scholar]
  212. LIOTTA I., MURINO P. Indagine statistica sulla frequenza della proprietà Cw nella popolazione residente nel Lazio. Policlinico Prat. 1956 Apr 23;63(17):572–574. [PubMed] [Google Scholar]
  213. LITCHFIELD H. R., WAGNER H. H. Familial autonomic dysfunction; Riley-Day syndrome. Arch Pediatr. 1956 Jan;73(1):1–5. [PubMed] [Google Scholar]
  214. LIVINGSTON S. O., CARR R. E. Hereditary hemorrhagic telangiectasia; report of a case with hemothorax. J Thorac Surg. 1956 Apr;31(4):497–503. [PubMed] [Google Scholar]
  215. LUERS T., NACHTSHEIM H., PETZEL G. Phänokopie des Blutbildes des homozygoten Pelgers infolge reaktiver Linksverschiebung bei einem heterozygoten Pelger. Blut. 1956 Jul;2(3):177–187. doi: 10.1007/BF01630044. [DOI] [PubMed] [Google Scholar]
  216. LUNDEVALL J. The Kidd blood group system investigated with anti-JKa. Acta Pathol Microbiol Scand. 1956;38(1):39–42. doi: 10.1111/j.1699-0463.1956.tb03159.x. [DOI] [PubMed] [Google Scholar]
  217. MAKLEY T. A., Jr Heterochromic cyclitis in identical twins. Am J Ophthalmol. 1956 May;41(5):768–772. doi: 10.1016/0002-9394(56)91769-x. [DOI] [PubMed] [Google Scholar]
  218. MANN I., TURNER C. Color vision in native races in Australasia. Am J Ophthalmol. 1956 May;41(5):797–800. doi: 10.1016/0002-9394(56)91772-x. [DOI] [PubMed] [Google Scholar]
  219. MARCHAND L., BOREL J., LAROCHE J., GANRY C. Idiotie infantile familiale de Tay-Sachs, forme myoclono-épileptique chez deux frères; considérations cliniques, anatomo-pathologiques et héréditaires. Encephale. 1956;45(1):1–40. [PubMed] [Google Scholar]
  220. MARCHAND L., LOO P., ELOY G., DUFLOT J. P. Maladie d'Alzheimer, diagnostiquée cliniquement maladie de Pick. Ann Med Psychol (Paris) 1956 May;114(5):810-5; discussion, 815-6. [PubMed] [Google Scholar]
  221. MARGOLIUS A., Jr, RATNOFF O. D. Observations on the hereditary nature of Hageman trait. Blood. 1956 Jun;11(6):565–569. [PubMed] [Google Scholar]
  222. MARIE J., BRICAIRE H., SALET J. Forme familiale d'hyperplasie congénitale des capsules surrénales. 1956 Jun 22-Jul 6Bull Mem Soc Med Hop Paris. 72(21-23):689–691. [PubMed] [Google Scholar]
  223. MARKS H. H. Glycosuria, family history of diabetes, and life insurance; recent insurance mortality experience. Diabetes. 1956 Mar-Apr;5(2):130–136. doi: 10.2337/diab.5.2.130. [DOI] [PubMed] [Google Scholar]
  224. MATOTH Y. Thalassemia among Kurdistan Jews. Harefuah. 1955 Sep 1;49(5):87–89. [PubMed] [Google Scholar]
  225. MATRAS A., KOHLER J. Ein Beitrag zum Werner-Syndrom. Wien Med Wochenschr. 1956 May 19;106(20):437–441. [PubMed] [Google Scholar]
  226. MATSUNAGA E., EBBING H. C. Uber Ohrschmalztypen bei Deutschen und Japanern; Häufigkeit und Vererbung, Anwendbarkeit in der Vaterschaftsbegutachtung. Z Mensch Vererb Konstitutionsl. 1956;33(5):404–408. [PubMed] [Google Scholar]
  227. MATSUNAGA E. Selektion durch Unverträglichkeit im ABO-Blutgruppensystem zwischen Mutter und Fetus; Beiträge zu Auslese- und Kompensationsvorgängen. Blut. 1956 Jul;2(3):188–198. doi: 10.1007/BF01630045. [DOI] [PubMed] [Google Scholar]
  228. MAURICE P., RULLIERE R., ACAR J., LENEGRE J. Etude clinique de 90 cas de fibrillation auriculaire idiopathique. Bull Mem Soc Med Hop Paris. 1956 Jun 8;72(19-20):607–614. [PubMed] [Google Scholar]
  229. MAYOR L. Grupos sanguíneos em Angola. An Inst Med Trop (Lisb) 1953 Dec;10(4 Pt 2):3553–3556. [PubMed] [Google Scholar]
  230. MCBURNEY R. P., SANDERS R. L. Familial polyposis of the colon. Am Surg. 1956 Jun;22(6):583–594. [PubMed] [Google Scholar]
  231. MCCONNELL R. B., PYKE D. A., ROBERTS J. A. F. Blood groups in diabetes mellitus. Br Med J. 1956 Apr 7;1(4970):772–776. doi: 10.1136/bmj.1.4970.772. [DOI] [PMC free article] [PubMed] [Google Scholar]
  232. MCKUSICK V. A. Heritable disorders of connective tissue. V. Osteogenesis imperfecta. J Chronic Dis. 1956 Feb;3(2):180–202. doi: 10.1016/0021-9681(56)90113-8. [DOI] [PubMed] [Google Scholar]
  233. MCKUSICK V. A. Heritable disorders of connective tissue. VI. Pseudoxanthoma elasticum. J Chronic Dis. 1956 Mar;3(3):263–283. doi: 10.1016/0021-9681(56)90122-9. [DOI] [PubMed] [Google Scholar]
  234. MCKUSICK V. A. Heritable disorders of connective tissue. VII. The Hurler syndrome. J Chronic Dis. 1956 Apr;3(4):360–389. doi: 10.1016/0021-9681(56)90138-2. [DOI] [PubMed] [Google Scholar]
  235. MCNALLY P. A. Friedreich's ataxia and cardiac disease. Ir J Med Sci. 1956 Jul;(367):317–319. doi: 10.1007/BF02951115. [DOI] [PubMed] [Google Scholar]
  236. MOORHOUSE J. A., MATHEWSON F. A. Familial haemolytic anaemia: concurrent crises in three members of a family. Can Med Assoc J. 1956 Jul 15;75(2):133–135. [PMC free article] [PubMed] [Google Scholar]
  237. MORGAN W. T., WATKINS W. M. The production of the human blood group A and B genes in individuals belonging to group AB. Nature. 1956 Mar 17;177(4507):521–522. doi: 10.1038/177521a0. [DOI] [PubMed] [Google Scholar]
  238. MORICARD R., ONARIR R. Variations du nombre des chromosomes dans un même épithélioma pavimenteux cervical. Bull Fed Soc Gynecol Obstet Lang Fr. 1955;7(5):523–525. [PubMed] [Google Scholar]
  239. MORI P. A., HOLT J. F. Cranial manifestations of familial metaphyseal dysplasia. Radiology. 1956 Mar;66(3):335–343. doi: 10.1148/66.3.335. [DOI] [PubMed] [Google Scholar]
  240. MORTENSEN O., SONDERGAARD G. Galactosaemia. Acta Paediatr. 1955 Mar;44(2):155–162. doi: 10.1111/j.1651-2227.1955.tb04126.x. [DOI] [PubMed] [Google Scholar]
  241. MOSELEY J. E., MOLOSHOK R. E. Pulmonary roentgen findings in familial dysautonomia. J Mt Sinai Hosp N Y. 1956 May-Jun;23(3):306–317. [PubMed] [Google Scholar]
  242. MOTEN A. N., STEWART G. T. Blood groups of Muslims and Parsees in Pakistan. Br J Haematol. 1956 Jan;2(1):61–64. doi: 10.1111/j.1365-2141.1956.tb06684.x. [DOI] [PubMed] [Google Scholar]
  243. MOULLEC J. Le facteur Rh dans la pratique quotidienne; le problème des variantes Du. Sem Hop. 1956 Jan 30;32(7):389–392. [PubMed] [Google Scholar]
  244. NA-NAKORN S., BANGKOK, THAILAND, MINNICH V., CHERNOFF A. I. Studies on hemoglobin E. II. The incidence of hemoglobin E in Thailand. J Lab Clin Med. 1956 Mar;47(3):490–498. [PubMed] [Google Scholar]
  245. NAGER G. T. Ein Paar weiblicher eineilger Zwillinge mit klinisch sowle anatomisch konkordanter Otosklerose und ähnlichem Hörgewinn durch Fenestration. Acta Otolaryngol. 1955 Jan-Feb;45(1):42–58. doi: 10.3109/00016485509118142. [DOI] [PubMed] [Google Scholar]
  246. NAGURA S. Zur Atiologie des angeborenen Klumpfusses. Zentralbl Chir. 1956;81(5):187–196. [PubMed] [Google Scholar]
  247. NEEL J. V. The genetics of human haemoglobin differences: problems and perspectives. Ann Hum Genet. 1956 Jul;21(1):1–30. [PubMed] [Google Scholar]
  248. NERI SERNERI G. G., BARTOLI V. Sulla eredopatologia delle mesenchimopatie reattive (cosidette malattie del collageno). I. Ricerche cui fattori ereditari del reumatismo acuto primario. Acta Genet Med Gemellol (Roma) 1956 May;5(2):155–189. [PubMed] [Google Scholar]
  249. NILSSON L., RYTTINGER L. Oförutsedda Rh-immuniseringar. Sven Lakartidn. 1956 Mar 29;53(13):821–824. [PubMed] [Google Scholar]
  250. NOLL L. E., KONUGRES A. Dual isosensitization in dizygotic twins. Obstet Gynecol. 1956 Apr;7(4):385–389. [PubMed] [Google Scholar]
  251. NONNENMACHER H. Beitrag zum Glioma retinae, seiner Erblichkeit und Behandlung. Klin Monbl Augenheilkd Augenarztl Fortbild. 1955;127(6):735–746. [PubMed] [Google Scholar]
  252. NORDLING C. O. Evidence regarding the multiple mutation theory of the cancer-inducing mechanism. Acta Genet Stat Med. 1955;5(2):93–104. doi: 10.1159/000150766. [DOI] [PubMed] [Google Scholar]
  253. OSBORN S. B., SMITH E. E. The genetically significant radiation dose from the diagnostic use of x-rays in England and Wales; a preliminary survey. Lancet. 1956 Jun 16;270(6929):949–953. doi: 10.1016/s0140-6736(56)91537-9. [DOI] [PubMed] [Google Scholar]
  254. OTTO F. M., PIETRUSCHKA G. Kongenitale familiäre Hämiglobinämie mit chronischen Augenveränderungen (Iridocyclitis, Cataracta complicata). Z Gesamte Inn Med. 1955 Dec 1;10(23-24):1110–1116. [PubMed] [Google Scholar]
  255. PALOMINO DENA F., NAVARRO G. Genética en oftalmología. Bol Med Hosp Infant Mex. 1956 Jan-Apr;13(1-2):489–522. [PubMed] [Google Scholar]
  256. PANNUTI M. La sindrome di Lawrence-Moon-Biedl; rivista sintetica. Osp Psichiatr. 1955 Oct-Dec;23(4):355–362. [PubMed] [Google Scholar]
  257. PAPARO F., PASETTI A. Coreo-atetosi doppia congenita in un solo membro di una coppia di gemelle identiche. Riv Neurol. 1956 Mar-Apr;26(2):205–207. [PubMed] [Google Scholar]
  258. PARKIN D. M. Study of a family with unusual ABO phenotypes. Br J Haematol. 1956 Jan;2(1):106–110. doi: 10.1111/j.1365-2141.1956.tb06692.x. [DOI] [PubMed] [Google Scholar]
  259. PARKS M. M. Strabismus; review of the literature for 1955. AMA Arch Ophthalmol. 1956 Jul;56(1):138–159. [PubMed] [Google Scholar]
  260. PARRINELLO G., BLANDINO G. Alterazioni scheletriche familiari da angiopatia periferica. Pediatria (Napoli) 1956 Jan-Feb;64(1):10–29. [PubMed] [Google Scholar]
  261. PARROW R. D. Hereditary cataract in two families. Acta Paediatr. 1955 Sep;44(5):460–464. doi: 10.1111/j.1651-2227.1955.tb04268.x. [DOI] [PubMed] [Google Scholar]
  262. PEEBLES BROWN D. A., MELROSE A. G., WALLACE J. The blood groups in peptic ulceration. Br Med J. 1956 Jul 21;2(4985):135–138. doi: 10.1136/bmj.2.4985.135. [DOI] [PMC free article] [PubMed] [Google Scholar]
  263. PENROSE L. S., SMITH S. M., SPROTT D. A. On the stability of allelic systems, with special reference to haemoglobins A, S and C. Ann Hum Genet. 1956 Jul;21(1):90–93. [PubMed] [Google Scholar]
  264. PICKERING D. E., KOULISCHER N. Discordance of cretinism in monozygotic twins. AMA J Dis Child. 1956 Jul;92(1):63–65. doi: 10.1001/archpedi.1956.02060030057013. [DOI] [PubMed] [Google Scholar]
  265. PICKERING G. W. The role of the genetic factor in hypertension. Acta Med Scand Suppl. 1956;312:18–27. doi: 10.1111/j.0954-6820.1956.tb16946.x. [DOI] [PubMed] [Google Scholar]
  266. PICKFORD R. W. Dominance order for red-green defective alleles. Nature. 1956 Jul 7;178(4523):49–50. doi: 10.1038/178049a0. [DOI] [PubMed] [Google Scholar]
  267. PLANANSKY K. Heredity in schizophrenia. J Nerv Ment Dis. 1955 Aug;122(2):121–142. doi: 10.1097/00005053-195508000-00001. [DOI] [PubMed] [Google Scholar]
  268. POLITZER W. M. Glucose-tolerance test: a comparison of results in the African and European. S Afr J Lab Clin Med. 1955 Dec;1(4):270–272. [PubMed] [Google Scholar]
  269. PONS J. Data on linkage in man: P.T.C. tasting and some dermatoglyphic traits. Ann Hum Genet. 1956 Jul;21(1):94–96. doi: 10.1111/j.1469-1809.1971.tb00268.x. [DOI] [PubMed] [Google Scholar]
  270. PONTONI L., IANNACCONE A. Attuali conoscenze sulla trasmissione ereditaria del diabete mellito. Prog Med (Napoli) 1956 Mar 31;12(6):161–168. [PubMed] [Google Scholar]
  271. POU PRADELL E. Parotiditis supurada en dos gemelos recién nacidos. Acta Pediatr Esp. 1956 Feb;14(158):104–106. [PubMed] [Google Scholar]
  272. RABSON S. M., MENDENHALL E. N. Familial hypertrophy of pineal body, hyperplasia of adrenal cortex and diabetes mellitus; report of 3 cases. Am J Clin Pathol. 1956 Mar;26(3):283–290. doi: 10.1093/ajcp/26.3.283. [DOI] [PubMed] [Google Scholar]
  273. RADAODY-RALAROSY P. A propos de l'éosinophilie tropicale essentielle; l'éosinophilie dans la bilharziose; cinq observations familiales. Bull Soc Pathol Exot Filiales. 1956 Jan-Feb;49(1):45-50; discussion, 50-1. [PubMed] [Google Scholar]
  274. RAPER A. B. Sickling in relation to morbidity from malaria and other diseases. Br Med J. 1956 Apr 28;1(4973):965–966. doi: 10.1136/bmj.1.4973.965. [DOI] [PMC free article] [PubMed] [Google Scholar]
  275. RAUCH S. Les facteurs constitutionnels et génétiques de la pneumatisation mastoïdienne. Rev Laryngol Otol Rhinol (Bord) 1956 Jan-Feb;77(1-2):68–83. [PubMed] [Google Scholar]
  276. RAWNSLEY H. M., YONAN V. L., REINHOLD J. G. Serum protein concentrations in the North American Negroid. Science. 1956 Jun 1;123(3205):991–992. doi: 10.1126/science.123.3205.991. [DOI] [PubMed] [Google Scholar]
  277. REESE A. B. Telangiectasis of the retina and Coats' disease. Am J Ophthalmol. 1956 Jul;42(1):1–8. doi: 10.1016/0002-9394(56)90002-2. [DOI] [PubMed] [Google Scholar]
  278. RICHARDS R. C., WOOLF C. Solitary polyps of the colon and rectum: a study of inherited tendency. Am Surg. 1956 Mar;22(3):287–294. [PubMed] [Google Scholar]
  279. RIEGER H. Neues aus der Erbpathologie des Auges. Klin Monbl Augenheilkd Augenarztl Fortbild. 1956;128(5):513–526. [PubMed] [Google Scholar]
  280. ROAF R. The natural history of deformities as seen in Northern India. Ann R Coll Surg Engl. 1956 Apr;18(4):211–227. [PMC free article] [PubMed] [Google Scholar]
  281. RUGGERI R., SOMAZZI D., CALVI N. Sulla sindrome di Laurence-Moon-Biedl-Bardet. G Psichiatr Neuropatol. 1955;83(4):913–934. [PubMed] [Google Scholar]
  282. RUKAVINA J. G., BLOCK W. D., CURTIS A. C. Ultracentrifugal analyses of serum lipoproteins in familial primary systemic amyloidosis. J Lab Clin Med. 1956 Mar;47(3):365–369. [PubMed] [Google Scholar]
  283. SADEK H. M., CHAIB S. A. Anemia hemolítica hereditária associada à esquistossomiase hèpatosplênica. Arq Cir Clin Exp. 1955 May-Jun;18(3):132–142. [PubMed] [Google Scholar]
  284. SAEMUNDSSON J. Ehlers-Danlos Syndrome; a congenital mesenchymal disorder. Acta Med Scand Suppl. 1956;312:399–408. [PubMed] [Google Scholar]
  285. SALOMONE P. Ancora in tema di idiozia amaurotica familiare; il tipo Bielschowsky; contributo casistico. Minerva Pediatr. 1956 Jun 16;8(23-24):794–799. [PubMed] [Google Scholar]
  286. SANDELIUS G. Ninety-nine year old monozygotic twins. J Gerontol. 1956 Apr;11(2):171–174. doi: 10.1093/geronj/11.2.171. [DOI] [PubMed] [Google Scholar]
  287. SARMENTO A. Grupos sanguíneos dos mestiços de Angola; subsídios para o seu estudo. An Inst Med Trop (Lisb) 1953 Dec;10(4 Pt 2):3549–3552. [PubMed] [Google Scholar]
  288. SASS J., ZUKOWSKI W. Wrodzona i rodzinnie wystepujaca moczówka prosta. Pol Tyg Lek (Wars) 1956 Apr 23;11(17):743–745. [PubMed] [Google Scholar]
  289. SATO K. Three cases of microlithiasis alveolaris pulmonum occurring in one family. Sci Rep Res Inst Tohoku Univ Med. 1955 Oct;6(3):391–399. [PubMed] [Google Scholar]
  290. SAVAGE D. A family history of uterine and gastro-intestinal cancer. Br Med J. 1956 Aug 11;2(4988):341–343. doi: 10.1136/bmj.2.4988.341. [DOI] [PMC free article] [PubMed] [Google Scholar]
  291. SAVIN L. H. Corneal dystrophy associated with congenital ichthyosis and allergic manifestations in male members of a family. Br J Ophthalmol. 1956 Feb;40(2):82–89. doi: 10.1136/bjo.40.2.82. [DOI] [PMC free article] [PubMed] [Google Scholar]
  292. SCHAEFER L. E., ADLERSBERG D. Genetic and epidemiologic studies in cholesterol metabolism: contributions of a prepaid medical care program. Am J Public Health Nations Health. 1956 Aug;46(8):966–969. doi: 10.2105/ajph.46.8.966. [DOI] [PMC free article] [PubMed] [Google Scholar]
  293. SCHIAVINI C. A. Cystinurie, cystinose et maladie de De Toni-Debré-Fanconi. Pediatrie. 1956;11(2):181–203. [PubMed] [Google Scholar]
  294. SCHMIDT H. Renaler Zwergwuchs mit Knochendeformitäten bei drei Geschwistern. Arch Kinderheilkd. 1955;151(2):157–170. [PubMed] [Google Scholar]
  295. SEMELAIGNE, HUREZ, BRAULT, BATTISTELLI Maladie des griffes du chat; épidémie familiale; coïncidence avec des èpizooties à virus. Arch Fr Pediatr. 1956;13(1):67–69. [PubMed] [Google Scholar]
  296. SIDDOO J. K., SIDDOO S. K., CHASE W. H., MORGAN-DEAN L., PERRY W. H. Thalassemia in Sikhs. Blood. 1956 Mar;11(3):197–210. [PubMed] [Google Scholar]
  297. SILVEIRA A. Aplicaço genética humana à higiene mental; revisão de 300 matrículas do Centro de Saúde de Santana. Arq Neuropsiquiatr. 1956 Jun;14(2):117–135. doi: 10.1590/s0004-282x1956000200002. [DOI] [PubMed] [Google Scholar]
  298. SIMMONS R. T., GRAYDON J. J., SEMPLE N. M., FRY E. I. A blood group genetical survey in Cook Islanders, Polynesia, and comparisons with American Indians. Am J Phys Anthropol. 1955 Dec;13(4):667–690. doi: 10.1002/ajpa.1330130409. [DOI] [PubMed] [Google Scholar]
  299. SKELLER E. Arcus senilis corneae: its frequency in some ethnic groups. Acta Ophthalmol (Copenh) 1955;33(5):623–626. doi: 10.1111/j.1755-3768.1955.tb03335.x. [DOI] [PubMed] [Google Scholar]
  300. SLOAN H., HAIGHT C. Congenital atresia of the esophagus in brothers. J Thorac Surg. 1956 Aug;32(2):209–215. [PubMed] [Google Scholar]
  301. SMETANA H. F., COHEN B. M. Mortality in relation to histologic type in Hodgkin's disease. Blood. 1956 Mar;11(3):211–224. [PubMed] [Google Scholar]
  302. SMILEY R. K., DEMPSEY H., VILLENEUVE P., CAMPBELL J. S. Atypical familial hemolytic anemia. Blood. 1956 Apr;11(4):324–337. [PubMed] [Google Scholar]
  303. SMITHIES O., WALKER N. F. Genetic control of some serum proteins in normal humans. Nature. 1955 Dec 31;176(4496):1265–1266. doi: 10.1038/1761265a0. [DOI] [PubMed] [Google Scholar]
  304. SOBERON ACEVEDO J., NERI R. J., CEPEDA DE LA PENA A., SAENZ ARROYO L. Miocardiopatía degenerativa familiar como entidad nosológica definida. Arq Bras Cardiol. 1956 Mar;9(1):24–40. [PubMed] [Google Scholar]
  305. SOHAR E. Renal disease, inner ear deafness, and ocular changes; a new heredofamilial syndrome. AMA Arch Intern Med. 1956 May;97(5):627–630. doi: 10.1001/archinte.1956.00250230121013. [DOI] [PubMed] [Google Scholar]
  306. SOLOMON R., BLISS E. L. Simultaneous occurrence of schizophrenia in identical twins. Am J Psychiatry. 1956 May;112(11):912–915. doi: 10.1176/ajp.112.11.912. [DOI] [PubMed] [Google Scholar]
  307. SOMMERS B. Problems in the clinical diagnosis and classification of ventricular hypertrophy in adults. III. Familial cardiopathy. Minn Med. 1956 Mar;39(3):153–156. [PubMed] [Google Scholar]
  308. SORSBY A., SAVORY M. Choroidal sclerosis; a possible intermediate sex-linked form. Br J Ophthalmol. 1956 Feb;40(2):90–95. doi: 10.1136/bjo.40.2.90. [DOI] [PMC free article] [PubMed] [Google Scholar]
  309. SORSBY A., SAVORY M., DAVEY J. B., FRASER R. J. L. Macular cysts; a dominantly inherited affection with a progressive course. Br J Ophthalmol. 1956 Mar;40(3):144–158. doi: 10.1136/bjo.40.3.144. [DOI] [PMC free article] [PubMed] [Google Scholar]
  310. STECHER R. M. Heredity of arthritis. Acta Med Scand Suppl. 1956;312:318–324. doi: 10.1111/j.0954-6820.1956.tb17004.x. [DOI] [PubMed] [Google Scholar]
  311. STEFANOVIC S., BOZOVIC B., MILOSAVLJEVIC A., VERBIC N., GUZINA Dj. Hemofilija AB - nova podgrupa hemofilije; povodom prvog slucaja. Srp Arh Celok Lek. 1956 Jan;84(1):59–66. [PubMed] [Google Scholar]
  312. STEIN W., KIKIELA M. Dwa rodzinne przypadki choroby Oguchiego. Klin Oczna. 1956;26(3):227–234. [PubMed] [Google Scholar]
  313. STEVENSON A. C., CHEESEMAN E. A. Hereditary deaf mutism, with particular reference to Northern Ireland. Ann Hum Genet. 1956 Feb;20(3):177–231. doi: 10.1111/j.1469-1809.1956.tb01367.x. [DOI] [PubMed] [Google Scholar]
  314. STUART C. Su alcune malformazioni della rotula nella stessa famiglia. Atti Accad Fisiocrit Siena Med Fis. 1955;2:88–96. [PubMed] [Google Scholar]
  315. STURTZ G. S., BURKE E. C. Hereditary hematuria, nephropathy and deafness; preliminary report. N Engl J Med. 1956 Jun 14;254(24):1123–1126. doi: 10.1056/NEJM195606142542404. [DOI] [PubMed] [Google Scholar]
  316. SUSSMAN L. N. Blood groups in Chinese of New York area; studies with A-B-O, M-N, Rh-Hr, Kell and P groups. Am J Clin Pathol. 1956 May;26(5):471–476. doi: 10.1093/ajcp/26.5.471. [DOI] [PubMed] [Google Scholar]
  317. SVEINSSON K. Glákusjúkdómur og aettgengi. Laeknabladid. 1956;40(1-2):1–14. [PubMed] [Google Scholar]
  318. SWAAK A. J. Pachyonychia congenita. Ned Tijdschr Geneeskd. 1956 Feb 18;100(7):486–488. [PubMed] [Google Scholar]
  319. SZELEI B. Osteopoikilia familiaris. Magy Radiol. 1956 May;8(2):89–94. [PubMed] [Google Scholar]
  320. TARACENA DEL PINAL B., DONADEU LUENGO J. Dos casos de enfermedad de Crouzon en hermanas. Acta Pediatr Esp. 1955 Nov;13(155):930–937. [PubMed] [Google Scholar]
  321. TEIXEIRA W. G., TEIXEIRA W. G. Contribuiço para o estudo dos grupos sanguíneos (sistema ABO) dos indígenas de Angola. An Inst Med Trop (Lisb) 1953 Dec;10(4 Pt 2):3541–3548. [PubMed] [Google Scholar]
  322. TELFER T. P., DENSON K. W., WRIGHT D. R. A new coagulation defect. Br J Haematol. 1956 Jul;2(3):308–316. doi: 10.1111/j.1365-2141.1956.tb06703.x. [DOI] [PubMed] [Google Scholar]
  323. TEODORI U., BORGHI A., NERI SERNERI G. G. Vererbung und Lokalisation von Krankheiten. Hippokrates. 1956 May 15;27(9):279–281. [PubMed] [Google Scholar]
  324. THAMBIPILLAI V. Taste threshold for phenyl-thio-urea in Malay school children. Ann Hum Genet. 1956 Feb;20(3):232–238. doi: 10.1111/j.1469-1809.1956.tb01368.x. [DOI] [PubMed] [Google Scholar]
  325. THORUP O. A., ITANO H. A., WHEBY M., LEAVELL B. S. Hemoglobin J. Science. 1956 May 18;123(3203):889–890. doi: 10.1126/science.123.3203.889. [DOI] [PubMed] [Google Scholar]
  326. TOBLER R., PRADER, TAILLARD, DEBRUNNER Die familiäre Vitamin D-resistente Rachitis. Ann Paediatr. 1956 Feb;186(2):91–92. [PubMed] [Google Scholar]
  327. TORRIOLI RIGGIO G., REGGIANI L. Morfologia dei polinucleati neutrofili studiata con il metodo gemellare. I. La formula di Arneth. Acta Genet Med Gemellol (Roma) 1956 May;5(2):125–137. [PubMed] [Google Scholar]
  328. TOWER P. The fundus oculi in monozygotic twins; report of six pairs of identical twins. AMA Arch Ophthalmol. 1955 Aug;54(2):225–239. doi: 10.1001/archopht.1955.00930020231010. [DOI] [PubMed] [Google Scholar]
  329. TRON E. Zh. K voprosu o nasledstvennosti elementov opticheskogo apparata glaza. Probl Fizol Opt. 1955;11:88–94. [PubMed] [Google Scholar]
  330. TRUBE-BECKER E. Zur Vererbung der A-Untergruppen. Dtsch Z Gesamte Gerichtl Med. 1956;44(6):724–732. [PubMed] [Google Scholar]
  331. UNGHVARY L., SCHULTHEIS E. Gemeinschaftliches Vorkommen von familiärer Ovalocytose und konstitutioneller Eosinophilie. Folia Haematol Int Mag Klin Morphol Blutforsch. 1955;73(2):134–135. [PubMed] [Google Scholar]
  332. VAN BEUKERING J. A., VERVOORN J. D. A case of uni-ovular twins of which one child was normal and the other had the syndrome of mongolism. Acta Genet Med Gemellol (Roma) 1956 Jan;5(1):113–114. doi: 10.1017/s1120962300027050. [DOI] [PubMed] [Google Scholar]
  333. VAN DER MEIREN L., MORIAME G. Acné congoblata et sébocystomatose familiale. Arch Belg Dermatol Syphiligr. 1955 Nov;11(2):155–158. [PubMed] [Google Scholar]
  334. VAN STRAATEN A. De thrombopathieën, vanuit genetisch standpunt bezien. Geneeskd Bl. 1955;47(8):241–266. [PubMed] [Google Scholar]
  335. VANDEPITTE J., MOTULSKY A. G. Abnormal haemoglobins in the Kasai province of the Belgian Congo. Nature. 1956 Apr 21;177(4512):757–757. doi: 10.1038/177757a0. [DOI] [PubMed] [Google Scholar]
  336. VECCHIO F., SCHETTINI F., PIOMELLI S. Su una nuova sindrome emorragica in una neonata deficit associato di PTC, fattore VII e protrombina. Pediatria (Napoli) 1956 Mar-Apr;64(2):188–201. [PubMed] [Google Scholar]
  337. VOGEL F., BALTHASER G. Uber ein männliches eineiiges Zwillingspaar mit angeborenem Nystagmus und Myopie. Klin Monbl Augenheilkd Augenarztl Fortbild. 1956;128(4):456–459. [PubMed] [Google Scholar]
  338. VOGEL F., WENDT G. G. Zwillingsuntersuchung über die Erblichkeit einiger anthropologischer Masse und Konstitutionsindices. Z Mensch Vererb Konstitutionsl. 1956;33(5):425–446. [PubMed] [Google Scholar]
  339. VOGT W. Untersuchungen zur Natur von H-Substanzen. Naunyn Schmiedebergs Arch Exp Pathol Pharmakol. 1956;228(1-2):200–201. [PubMed] [Google Scholar]
  340. VON KEYSERLINGK H. Zum familiären Vorkommen der idiopathischen Torsionsdystonie. Nervenarzt. 1956 Jan 20;27(1):34–35. [PubMed] [Google Scholar]
  341. VON KNORRE G. Uber die Myositis ossificans progressiva. Z Mensch Vererb Konstitutionsl. 1955;33(2):85–95. [PubMed] [Google Scholar]
  342. VON VERSCHUER O. F. Die genetischen Grundlagen der Sexualkonstitution des Menschen. Z Mensch Vererb Konstitutionsl. 1956;33(4):316–329. [PubMed] [Google Scholar]
  343. WAGNER W. Alopezie und Nagelverändergungen bei Epidermolysis bullosa hereditaria. Z Haut Geschlechtskr. 1956 May 15;20(10):278–285. [PubMed] [Google Scholar]
  344. WALSH R. J., KOOPTZOFF O. Blood groups and disease: rheumatic fever. Australas Ann Med. 1956 Feb;5(1):17–19. doi: 10.1111/imj.1956.5.1.17. [DOI] [PubMed] [Google Scholar]
  345. WALTERS J. H., LEHMANN H. Distribution of the S and C haemoglobin variants in two Nigerian communities. Trans R Soc Trop Med Hyg. 1956 May;50(3):204–208. doi: 10.1016/0035-9203(56)90024-4. [DOI] [PubMed] [Google Scholar]
  346. WALTON J. N. The inheritance of muscular dystrophy: further observations. Ann Hum Genet. 1956 Jul;21(1):40–58. doi: 10.1111/j.1469-1809.1971.tb00264.x. [DOI] [PubMed] [Google Scholar]
  347. WARBURG E. Clinical statistics of congenital cardiac disease; 1000 cases analyzed. Acta Med Scand Suppl. 1956;312:669–673. doi: 10.1111/j.0954-6820.1956.tb17070.x. [DOI] [PubMed] [Google Scholar]
  348. WARE G. W. Tetralogy of Fallot; review of literature. Clin Proc Child Hosp Dist Columbia. 1956 Feb;12(2):34–42. [PubMed] [Google Scholar]
  349. WARKANY J., FRASER F. C. The role of genetics and other prenatal factors in disorders of childhood; summary of round table discussion. Pediatrics. 1956 Aug;18(2):314–317. [PubMed] [Google Scholar]
  350. WHEBY M. S., THORUP O. A., LEAVELL B. S. Homozygous hemoglobin C disease in siblings: further comment on intraerythrocytic crystals. Blood. 1956 Mar;11(3):266–272. [PubMed] [Google Scholar]
  351. WHITTAKER S. R., WHITEHEAD T. P. Acute and latent porphyria. Lancet. 1956 Apr 28;270(6922):547–551. doi: 10.1016/s0140-6736(56)90601-8. [DOI] [PubMed] [Google Scholar]
  352. WIENER A. S., GORDON E. B. A hitherto undescribed human blood group Am. Br J Haematol. 1956 Jul;2(3):305–307. doi: 10.1111/j.1365-2141.1956.tb06702.x. [DOI] [PubMed] [Google Scholar]
  353. WINTER S. T., ZELTZER M. Congenital atresia of the ileum in two brothers; case report. J Pediatr. 1956 Aug;49(2):194–196. doi: 10.1016/s0022-3476(56)80035-8. [DOI] [PubMed] [Google Scholar]
  354. WISKEMANN A. Familiäres polymorphes Lichtexanthem. Arch Klin Exp Dermatol. 1956;202(4):325–330. [PubMed] [Google Scholar]
  355. WITKOP C. J., Jr, DYSON H. R., SACKETT L. M. A study of hereditary defects occurring in a racial isolate residing in Southern Maryland; special report. Clin Proc Child Hosp Dist Columbia. 1956 Feb;12(2):29–33. [PubMed] [Google Scholar]
  356. WIXSON R. J. Statistical analysis of hereditary factors in ametropia. Am J Optom Arch Am Acad Optom. 1956 Jul;33(7):374–379. doi: 10.1097/00006324-195607000-00005. [DOI] [PubMed] [Google Scholar]
  357. WU H. C. Laurence-Moon-Biedl syndrome; report of two cases. Chin Med J. 1956 Jan-Feb;74(1):75–80. [PubMed] [Google Scholar]
  358. YOUNG L. E. Observations on inheritance and heterogeneity of chronic spherocytosis. Trans Assoc Am Physicians. 1955;68:141–148. [PubMed] [Google Scholar]
  359. ZOUTENDYK A., KOPEC A. C., MOURANT A. E. The blood groups of the Hottentots. Am J Phys Anthropol. 1955 Dec;13(4):691–697. doi: 10.1002/ajpa.1330130410. [DOI] [PubMed] [Google Scholar]

Articles from American Journal of Human Genetics are provided here courtesy of American Society of Human Genetics

RESOURCES