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. 1953 Sep;5(3):284–291.

Bibliography of human genetics

PMCID: PMC1716477  PMID: 13080253

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Selected References

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

  1. ALDER A., SCHAUB F. Gleichzeitiges Vorkommen von Pelgerscher Kernanomalie und von Blutkrankheiten. Dtsch Med Wochenschr. 1952 Oct 17;77(42):1290–1293. doi: 10.1055/s-0028-1117220. [DOI] [PubMed] [Google Scholar]
  2. APPEL L., VAN BOGAERT L. Etudes sur la paraplégie spasmodique familiale. IV. La famille Fev...: forme très tardive; contribution histopathologique. Acta Neurol Psychiatr Belg. 1952 Mar;52(3):129–140. [PubMed] [Google Scholar]
  3. BAGGIO G. C., POZZAN M., SOSSAI M. Contributo alla conoscenza delle iperostosi corticali diafisarie del lattante; sindrome di Caffey a carattere familiare. Acta Paediatr Lat. 1952 Sep-Oct;5(5):481–496. [PubMed] [Google Scholar]
  4. BANKS L. O., SCOTT R. B., SIMMONS J. Studies in sickle cell anemia; inheritance factor, including effect of interaction of genes for sicklemia and thalassemia. AMA Am J Dis Child. 1952 Nov;84(5):601–608. doi: 10.1001/archpedi.1952.02050050075004. [DOI] [PubMed] [Google Scholar]
  5. BARTSOKAS S., PLATIS E., DERVENOULAS G. L'anemie à hematies falciformes chez l'homme blanc. Arch Fr Pediatr. 1952;9(7):709–710. [PubMed] [Google Scholar]
  6. BAUZA C. A., STABILE A., LYONNET A. Idiocia amaurótica familiar (enfermedad de Tay-Sachs). Arch Pediatr Urug. 1952 Oct;23(10):688–690. [PubMed] [Google Scholar]
  7. BECKER P. E. Eine klinisch-genetische Untersuchung der Dystrophia musulorum progressiva (Erb). Arch Psychiatr Nervenkr Z Gesamte Neurol Psychiatr. 1952;189(1):1–22. doi: 10.1007/BF00355704. [DOI] [PubMed] [Google Scholar]
  8. BEGG M. Selection of the genetic basis for an acquired character. Nature. 1952 Apr 12;169(4302):625–625. doi: 10.1038/169625a0. [DOI] [PubMed] [Google Scholar]
  9. BERARDINELLI W. Hermafroditismo verdadeiro. Med Cir Farm. 1952 May;193:185–195. [PubMed] [Google Scholar]
  10. BEREDAY M., COBB S. Relation of hereditary optic atrophy (leber) to the other familial degenerative diseases of central nervous system. AMA Arch Ophthalmol. 1952 Dec;48(6):669–680. doi: 10.1001/archopht.1952.00920010681001. [DOI] [PubMed] [Google Scholar]
  11. BERREY R., CARSON B. Erythroblastosis in one of dizygotic twins; a case report. J Med Assoc State Ala. 1952 May;22(3):79–80. [PubMed] [Google Scholar]
  12. BERTOYE P., MONNET P., BRET J., TOURAINE Cardiopathie congénitale chez des jumeaux dizzygotes par embryopathie. J Med Lyon. 1952 Apr 20;33(775):391–393. [PubMed] [Google Scholar]
  13. BIRDSELL J. B. On various levels of objectivity in genetical anthropology. Am J Phys Anthropol. 1952 Sep;10(3):355–362. doi: 10.1002/ajpa.1330100319. [DOI] [PubMed] [Google Scholar]
  14. BIRO I. Beiträge zu den ophthalmologischen Beziehungen der Blutsverwandtenehen. Klin Monbl Augenheilkd Augenarztl Fortbild. 1951;119(6):585–596. [PubMed] [Google Scholar]
  15. BOLGERT M., CANIVET J., LE SOURD M. Trois cas de porphyrie cutanée congénitale (maladie de Gunther) dans la même fratrie. Bull Soc Fr Dermatol Syphiligr. 1952 May-Jun;59(3):233–236. [PubMed] [Google Scholar]
  16. BOOK J. A. Fréquence de mutation de la chondrodystrophie et de l'épidermolyse bulleuse dans une population du sud de la Suède. J Genet Hum. 1952 May;1(1):24–26. [PubMed] [Google Scholar]
  17. BROWN R. J. K. A clinico-pathological study of cystinosis in two siblings. Arch Dis Child. 1952 Oct;27(135):428–433. doi: 10.1136/adc.27.135.428. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. CHILDS A. W., CROSE R. F., HENDERSON P. H. Glycogen disease of the heart; report of two cases occurring in siblings. Pediatrics. 1952 Aug;10(2):208–217. [PubMed] [Google Scholar]
  19. COBLENTZ B., MATHIVAT A. Sténose pulmonaire congénitale chez deux soeurs. Arch Mal Coeur Vaiss. 1952 Jun;45(6):490–495. [PubMed] [Google Scholar]
  20. COLLIER W. A., DE LA PARRA D. A. Sickle-cell trait in Surinam creoles. Doc Med Geogr Trop. 1952 Sep;4(3):223–224. [PubMed] [Google Scholar]
  21. COLLIER W. A., FROS J., SCHIPPER J. F. A. Blood groups of some American Indian settlements. Doc Med Geogr Trop. 1952 Sep;4(3):225–226. [PubMed] [Google Scholar]
  22. COMFORT M. W., STEINBERG A. G. Pedigree of a family with hereditary chronic relapsing pancreatitis. Gastroenterology. 1952 May;21(1):54–63. [PubMed] [Google Scholar]
  23. CORDIER J., LOWENTHAL A., RADERMECKER M. A., VAN BOGAERT L. V. Sur une forme congénitale et héréditaire de sclérose musculaire généralisée: la famille Duc. Acta Neurol Psychiatr Belg. 1952 Jul;52(7):422–432. [PubMed] [Google Scholar]
  24. CRIGLER J. F., Jr, NAJJAR V. A. Congenital familial nonhemolytic jaundice with kernicterus. Pediatrics. 1952 Aug;10(2):169–180. [PubMed] [Google Scholar]
  25. DAHR P. Fünfzig Jahre ABO-Blutgruppensystem. Munch Med Wochenschr. 1952 May 2;94(18):930–935. [PubMed] [Google Scholar]
  26. DAVIDSOHN I., LEVINE P., WIENER A. S. Medicolegal application of blood grouping tests. J Am Med Assoc. 1952 Jun 14;149(7):699–706. [PubMed] [Google Scholar]
  27. DE GRACIANSKY P., BALTER, LEFORT Xanthomes multiples chez un albinos. Bull Soc Fr Dermatol Syphiligr. 1951 Nov-Dec;58(5):479–481. [PubMed] [Google Scholar]
  28. DURNIN J. V., WEIR J. B. Statures of a group of university students and of their parents. Br Med J. 1952 May 10;1(4766):1006–1008. doi: 10.1136/bmj.1.4766.1006. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. ELBEL H. Uber die Genetik der menschlichen Blutgruppen. Dtsch Z Gesamte Gerichtl Med. 1952;41(2):186–193. [PubMed] [Google Scholar]
  30. ENGLERT E., Jr, WARSHAW L. J. Familial mediterranean (Cooley's) anemia complicated by chronic hepatitis; results of treatment with ACTH. Am J Med. 1952 Oct;13(4):507–516. doi: 10.1016/0002-9343(52)90334-3. [DOI] [PubMed] [Google Scholar]
  31. EWALD G. Fetischismus und Anlage. Arch Psychiatr Nervenkr Z Gesamte Neurol Psychiatr. 1952 Oct 4;189(2):93–108. [PubMed] [Google Scholar]
  32. FADDA F. Grupos y subgrupos del factor Rh. Rev Chil Pediatr. 1952 Jan;23(1):41–42. [PubMed] [Google Scholar]
  33. FISHER G. Tératogénèse, génétique, embryogénèse et chimiotératogénèse. Concours Med. 1952 Aug 2;74(31):2735–2736. [PubMed] [Google Scholar]
  34. FOSSEL M., TROJAN R. Zur Beweiskraft der morphologisch-erbbiologischen Untersuchung und Feststellung der Zeugungsfähigkeit. Dtsch Z Gesamte Gerichtl Med. 1951;40(5):448–451. [PubMed] [Google Scholar]
  35. FRANCESCHETTI A., KOENIG H. L'importance du facteur hérédo-dégéneratif dans l'hémiatrophie faciale progressive (Romberg); étude des complications oculaires dans ce syndrome. J Genet Hum. 1952 May;1(1):27–64. [PubMed] [Google Scholar]
  36. GALDSTON M., STEELE J. M., DOBRINER K. Alcaptonuria and ochronosis; with a report of three patients and metabolic studies in two. Am J Med. 1952 Oct;13(4):432–452. doi: 10.1016/0002-9343(52)90298-2. [DOI] [PubMed] [Google Scholar]
  37. GAUTIER P., GUINAND-DONIOL J. Un syndrome nouveau; la maladie de Lobstein associée à la thrombasthénie familiale et héréditaire de Glanzmann. Schweiz Med Wochenschr. 1952 Apr 12;82(15):407–409. [PubMed] [Google Scholar]
  38. GILG I. Boeck's sarcoid in identical twins. Acta Derm Venereol Suppl (Stockh) 1952;32(29):108–115. [PubMed] [Google Scholar]
  39. GRAY F. G., QUINN R. W., QUINN J. P. A long-term survey of rheumatic and non-rheumatic families; with particular reference to environment and heredity. Am J Med. 1952 Oct;13(4):400–412. doi: 10.1016/0002-9343(52)90294-5. [DOI] [PubMed] [Google Scholar]
  40. GREBE H. Gibt es eine recessiv erbliche Chondrodysplasie (Chondrodystrophia foetalis, Achondroplasie)? Z Kinderheilkd. 1952 Aug;71(5):437–447. [PubMed] [Google Scholar]
  41. GROVE-RASMUSSEN M., SOUTTER L., LEVINE P. A new blood subgroup (Ao) identifiable with group O serums. Am J Clin Pathol. 1952 Dec;22(12):1157–1163. doi: 10.1093/ajcp/22.12.1157. [DOI] [PubMed] [Google Scholar]
  42. HAVERKAMP BEGEMANN N., VAN LOOKEREN CAMPAGNE A. Homozygous form of Pelger-Huët's nuclear anomaly in man. Acta Haematol. 1952 May;7(5):295–303. doi: 10.1159/000204063. [DOI] [PubMed] [Google Scholar]
  43. HEBEL R. Familiäre Häufung der Kartagener Trias. Z Laryngol Rhinol Otol. 1952 Feb;31(2):83–90. [PubMed] [Google Scholar]
  44. HERVE Quelques considérations à propos du chapitre antécédents héréditaires de l'observation clinique de prothèse totale. Rev Odontol Parana. 1951 Dec;73(12):549–552. [PubMed] [Google Scholar]
  45. HEYMAN A., PATTERSON J. L., Jr, DUKE T. W. Cerebral circulation and metabolism in sickle cell and other chronic anemias, with observations on the effects of oxygen inhalation. J Clin Invest. 1952 May;31(9):824–828. doi: 10.1172/JCI102668. [DOI] [PMC free article] [PubMed] [Google Scholar]
  46. HOLLY P. B., FELTS W. R., Jr, RHEINGOLD J. J. Pernicious anemia occurring simultaneously in identical Negro twins. AMA Arch Intern Med. 1952 Nov;90(5):707–710. doi: 10.1001/archinte.1952.00240110133011. [DOI] [PubMed] [Google Scholar]
  47. HUTCHESON J. B., HABER J. M., KELLNER A. A hazard of repeated blood transfusions; hemolytic reaction due to antibodies to the Duffy (Fya) factor. J Am Med Assoc. 1952 May 17;149(3):274–275. doi: 10.1001/jama.1952.72930200017011i. [DOI] [PubMed] [Google Scholar]
  48. JACOBSEN A. W., MACKLIN M. T. Hereditary sexual precocity; report of a family with 27 affected members. Pediatrics. 1952 Jun;9(6):682–695. [PubMed] [Google Scholar]
  49. JANKOVIC B. Rh antitela i njihov klini6cki zna6caj. Srp Arh Celok Lek. 1952 Jan;80(1):63–70. [PubMed] [Google Scholar]
  50. KNOLL H. A. Color vision differences in the two eyes of a given individual; a case of simulated unilateral atypical achromatopsia. Am J Optom Arch Am Acad Optom. 1952 Oct;29(10):539–542. [PubMed] [Google Scholar]
  51. KNOLL H. Wahnbildende Psychosen der Zeit des Klimakteriums und der Involution in klinischer und genealogischer Betrachtung. Arch Psychiatr Nervenkr Z Gesamte Neurol Psychiatr. 1952;189(1):59–92. doi: 10.1007/BF00355707. [DOI] [PubMed] [Google Scholar]
  52. KRAH E., WILDHAGEN K. Unspezifische Agglutinationen bei der Blutgruppenuntersuchung an menschlichem Fetalblut. Klin Wochenschr. 1952 Jul 1;30(25-26):610–611. doi: 10.1007/BF01471423. [DOI] [PubMed] [Google Scholar]
  53. KRYNSKI S., ARMINATE J. C., MILETTO A. Anemia falciforme; consideraçes neuro-psiquiátricas e hematólogicas a propósito de um caso. Hospital (Rio J) 1952 May;41(5):677–700. [PubMed] [Google Scholar]
  54. KULENKAMPFF D. Uber die Behandlung des Rhinophyms und des Zungenkropfes; ein Beitrag zur Genpathologie. Chirurg. 1952 Sep;23(9):405–410. [PubMed] [Google Scholar]
  55. KUPPERMAN H. G., BARTFELD H. Rheumatoid spondylitis treated with cortisone; heredity and effect on pregnancy. N Y State J Med. 1952 May 1;52(9):1157–1159. [PubMed] [Google Scholar]
  56. LEHMANN W. Das erbbiologische Gutachten. Dtsch Z Gesamte Gerichtl Med. 1952;41(2):173–185. [PubMed] [Google Scholar]
  57. MACMAHON B., MCKEOWN T. A note on the sex ratio in anencephalus. Br J Soc Med. 1952 Oct;6(4):265–266. doi: 10.1136/jech.6.4.265. [DOI] [PMC free article] [PubMed] [Google Scholar]
  58. MAGGIORE L. I matrimoni fra consanguinei: pericoli per la integrità dei discendenti; l'importanza ed il significato del fattore consanguineità dei genitori nella genesi di talune forme morbose ereditarie dell'apparato visivo. Athena. 1952 Jul-Aug;18(7-8):303–305. [PubMed] [Google Scholar]
  59. MCEVITT W. G. Cleft lip and palate and parental age; a statistical study of etiology. Plast Reconstr Surg (1946) 1952 Aug;10(2):77–82. doi: 10.1097/00006534-195208000-00003. [DOI] [PubMed] [Google Scholar]
  60. MERTINS H. Uber eine familiäre Zwerchfellmissbildung. Zentralbl Gynakol. 1952;74(24):951–955. [PubMed] [Google Scholar]
  61. MOLLA W. Comportamento dell'antigene A nei gruppi AB. Sangue. 1952 Jan-Feb;25(1):4–13. [PubMed] [Google Scholar]
  62. MOORRESS C. F. A., OSBORNE R. H., WILD E. Torus mandibularis: its occurrence in Aleut children and its genetic determinants. Am J Phys Anthropol. 1952 Sep;10(3):319–329. doi: 10.1002/ajpa.1330100317. [DOI] [PubMed] [Google Scholar]
  63. MORTELMANS L. Forme familiale de la dystrophie cornéenne de Fuchs. Ophthalmologica. 1952 Feb;123(2):88–99. doi: 10.1159/000301139. [DOI] [PubMed] [Google Scholar]
  64. MULLER H. J. Strahlenschädigung des genetischen Materials. Strahlentherapie. 1951;85(4):509–536. [PubMed] [Google Scholar]
  65. NAYRAC P., HOUCKE E., BISERTE G., RABACHE R. Dégénérescence hépatolenticulaire chez la soeur et le frère; ponction-biopsie du foie; amino-acidurie. Rev Neurol (Paris) 1951;85(5):388–392. [PubMed] [Google Scholar]
  66. PFANDLER U. La voie de la Génetique du Micromérisme a l'Atomisme biologique. Schweiz Med Wochenschr. 1952 Mar 8;82(10):258–260. [PubMed] [Google Scholar]
  67. PHANSOMBOON S., POLLAK O. J. A study on the A factor as a cause of haemolytic disease in premature babies. Br Med J. 1952 May 31;1(4769):1170–1172. doi: 10.1136/bmj.1.4769.1170. [DOI] [PMC free article] [PubMed] [Google Scholar]
  68. PHILIPP E. E., SKELTON M. O. Congenital diaphragmatic hernia in siblings. Br Med J. 1952 Jun 14;1(4771):1283–1284. doi: 10.1136/bmj.1.4771.1283. [DOI] [PMC free article] [PubMed] [Google Scholar]
  69. PORTIER A., MASSONNAT J. Epilepsie et syndrome hématologique méditérranéen. Presse Med. 1952 Mar 22;60(19):395–396. [PubMed] [Google Scholar]
  70. PROCHAZKA J. Vrozené kycelní dysplasie u trojcat. Acta Chir Orthop Traumatol Cech. 1952;19(4-8):245–251. [PubMed] [Google Scholar]
  71. PROPPE A. Geschlechtsgebundene Dermatosen. Z Haut Geschlechtskr. 1952 Sep 15;13(6):166–174. [PubMed] [Google Scholar]
  72. RABASA S. L. Base genética de algunas enfermedades de la sangre. Pediatr Am. 1951 Aug;9(8):343–353. [PubMed] [Google Scholar]
  73. REILLY E. B., RAPAPORT S. I., KARR N. W., MILLS H., CARPENTER G. E. Familial chronic lymphatic leukemia. AMA Arch Intern Med. 1952 Jul;90(1):87–89. doi: 10.1001/archinte.1952.00240070093009. [DOI] [PubMed] [Google Scholar]
  74. RISETTI U., PROPERZI E. Infantilo-nanismo diencefalo-ipofisario atipico con carattere familiare, aracnodattilia e malformazioni multiple. Folia Endocrinol Mens Incretologia Incretoterapia. 1952 Feb;5(1):77–106. [PubMed] [Google Scholar]
  75. ROBERTS M. H., BAEHREN P. F. Adrenocortical insufficiency observed in three male infants in one family. J Med Assoc Ga. 1952 May;41(7):299–304. [PubMed] [Google Scholar]
  76. ROCHA J. M. D., CASTRO A. S. D. Enfermedades sanguineas de tendencia hemorragipara; sindromos hemorragiparos familiares. Arch Pediatr Urug. 1952 Oct;23(10):704–706. [PubMed] [Google Scholar]
  77. ROLLINS W. C., COLE H. H. The relative importance of genetic and environmental factors in determining the precision of gonadotrophin assay. Endocrinology. 1952 Sep;51(3):203–209. doi: 10.1210/endo-51-3-203. [DOI] [PubMed] [Google Scholar]
  78. ROUSSET J. Génodermatose difficilement classable (trichorrhexis nodosa) prédominant chez les mâles dans quatre générations. Bull Soc Fr Dermatol Syphiligr. 1952 May-Jun;59(3):298–300. [PubMed] [Google Scholar]
  79. RUEDEMANN A. D., Jr Osteogenesis imperfecta congenita and blue sclerotics; a clinicopathologic study. AMA Arch Ophthalmol. 1953 Jan;49(1):6–16. doi: 10.1001/archopht.1953.00920020009002. [DOI] [PubMed] [Google Scholar]
  80. Rapp G. W., Richardson G. C. A Saliva Test for Prenatal Sex Determination. Science. 1952 Mar 7;115(2984):265–265. doi: 10.1126/science.115.2984.265. [DOI] [PubMed] [Google Scholar]
  81. SANGUINETI I. Contributo allo studio delle sindromi distrofiche eredo-familiari; su un caso di associazione dell'amiotrofia tipo Charcot-Marie con il morbo di Friedreich. Sist Nerv. 1950 Mar-Apr;2(2):141–144. [PubMed] [Google Scholar]
  82. SCHACHTER M. Syndrome schizophreniforme et oligophrenique infantile, précoce, rôle des facteurs constitutionnels, gestatifs et post-nataux. Sist Nerv. 1950 Mar-Apr;2(2):87–92. [PubMed] [Google Scholar]
  83. SCHAFFER R. C. Familial colonic polyposis; review of the literature and report of four cases. Am J Surg. 1952 Oct;84(4):477–482. doi: 10.1016/0002-9610(52)90020-2. [DOI] [PubMed] [Google Scholar]
  84. SCHOCKAERT R., JANSSENS J. Hydrocéphalies congénitales répétées. Bull Fed Soc Gynecol Obstet Lang Fr. 1951;3(4):560–566. [PubMed] [Google Scholar]
  85. SCHWARTZ M. Heredity in bronchial asthma; a clinical and genetic study of 191 asthma probands and 50 probands with Baker's asthma. Acta Allergol Suppl (Copenh) 1952;2:1–288. [PubMed] [Google Scholar]
  86. SCHWARZ G. A. Hereditary (familial) spastic paraplegia. AMA Arch Neurol Psychiatry. 1952 Nov;68(5):655–662. doi: 10.1001/archneurpsyc.1952.02320230081010. [DOI] [PubMed] [Google Scholar]
  87. SELBY E. R. Hereditary transmission of physical defects in the EMB family. Can Med Assoc J. 1952 May;66(5):439–441. [PMC free article] [PubMed] [Google Scholar]
  88. STOBBE H., TAESCHNER H. Konkordantes Auftreten lymphatischer Leukämie bei eineiigen Zwillingen; Beitrag zur familiären Leukose. Z Gesamte Inn Med. 1952 Aug 15;7(16):736–739. [PubMed] [Google Scholar]
  89. TESORO J. Los factores Rh sanguineos. Dia Med. 1952 Mar 10;24(10):200–204. [PubMed] [Google Scholar]
  90. THORSEN H. U. Et tilfelle av odontogenesis imperfekta hereditaria. Nor Tannlaegeforen Tid. 1952 Feb;62(2):67–71. [PubMed] [Google Scholar]
  91. TORGERSEN J. The Triad of Kartagener; a contribution to its hereditary and developmental basis. Schweiz Med Wochenschr. 1952 Jul 26;82(30):770–771. [PubMed] [Google Scholar]
  92. TOURAINE A. Utilité de publier de nombreuses observations de génétique médicale. Gaz Med Port. 1952;5(1):91–95. [PubMed] [Google Scholar]
  93. TRAMPUZ V. Fetomaterna krvna inkompatibilnost po sistemu-ABO. Zdrav Vestn. 1952;21(3-4):54–57. [PubMed] [Google Scholar]
  94. TRINCAO C., SOARES A. D., LANCA J. B., FLORA A. Ictericia não hemolitica familiar. Gaz Med Port. 1952;5(3):339–348. [PubMed] [Google Scholar]
  95. TUCHMANN-DUPLESSIS H. L'hérédité pathologique. Concours Med. 1952 Jul 12;74(28):2561–2564. [PubMed] [Google Scholar]
  96. TUCHMANN-DUPLESSIS H. Les bases expérimentales du déterminisme et de la différenciation sexuelle. II. Vertébrés. Concours Med. 1952 May 24;74(21):1973–1975. [PubMed] [Google Scholar]
  97. TURPIN R., SENECAL J., SCHUTZENBERGER M. P. Consanguinité et tuberculose. Bull Acad Natl Med. 1952 Jan 8;136(1-2):10–12. [PubMed] [Google Scholar]
  98. VAN BOGAERT L. Etude génétique sur les paraplégies spasmodiques familiales. J Genet Hum. 1952 May;1(1):6–23. [PubMed] [Google Scholar]
  99. VAN GEERTRUYDEN E. Premiere observation belge de la malformation congénitale de Ullrich-Bonnevie. Acta Neurol Psychiatr Belg. 1952 Feb;52(2):102–110. [PubMed] [Google Scholar]
  100. VAUGHAN V. C., 3rd, ALLEN F. H., Jr, DIAMOND L. K. Variability in erythroblastosis fetalis: a study of multiple pregnancies and of twins. AMA Am J Dis Child. 1952 Dec;84(6):739–740. [PubMed] [Google Scholar]
  101. VOLPE A., RAMON GUERRA A. U., ESCANDE C. A., BOCCOLERI C. S. Síndromo de anemia aplasica (panhematopenia) familiar asociado a hipocrecimiento y diabetes renal. Arch Pediatr Urug. 1952 Oct;23(10):715–716. [PubMed] [Google Scholar]
  102. VON VERSCHUER O. Erbforschung am Menschen-neuere Ergebnisse und Erkenntnisse. Dtsch Med Wochenschr. 1952 Oct 10;77(41):1245–1248. doi: 10.1055/s-0028-1117204. [DOI] [PubMed] [Google Scholar]
  103. WAARDENBURG P. J. Angio-sclérose familiale de la choroïde. J Genet Hum. 1952 May;1(1):83–90. [PubMed] [Google Scholar]
  104. WADDINGTON C. H. Selection of the genetic basis for an acquired character. Nature. 1952 Apr 12;169(4302):625–626. doi: 10.1038/169625b0. [DOI] [PubMed] [Google Scholar]
  105. WADE G. Congenital heart disease in one of uniovular twins. Br Heart J. 1952 Oct;14(4):475–480. doi: 10.1136/hrt.14.4.475. [DOI] [PMC free article] [PubMed] [Google Scholar]
  106. WEISS A. Blutdruck und erbliche Lebenserwartung. Arch Kreislaufforsch. 1952 Sep;18(7-10):301–322. [PubMed] [Google Scholar]
  107. WHITTEN W. W., ADIE G. C. Congenital biliary atresia; report of three cases; two occurring in one family. J Pediatr. 1952 May;40(5):539–548. doi: 10.1016/s0022-3476(52)80143-x. [DOI] [PubMed] [Google Scholar]
  108. WILLIAMS D. I. The diagnosis of intersex. Br Med J. 1952 Jun 14;1(4771):1264–1270. doi: 10.1136/bmj.1.4771.1264. [DOI] [PMC free article] [PubMed] [Google Scholar]
  109. ZUNIN C. Contributo alla conoscenza dello status Bonnevie-Ullrich. Minerva Pediatr. 1951 Oct;3(10):547–557. [PubMed] [Google Scholar]

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