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. 1966 Jul;18(4):374–386.

Frequency and occurrence of chromosomal syndromes. I. D-Trisomy.

P E Conen, B Erkman
PMCID: PMC1706101  PMID: 5945953

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Selected References

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

  1. ATKINS L., ROSENTHAL M. K. Multiple congenital abnormalities associated with chromosomal trisomy. N Engl J Med. 1961 Aug 17;265:314–318. doi: 10.1056/NEJM196108172650703. [DOI] [PubMed] [Google Scholar]
  2. BLANCK C., JALLING B., LINDSTEN J., ZETTERQVIST TRISOMY 13-15. REPORT OF A CASE WITH CLINICAL, CYTOGENETIC AND PATHOLOGIC FINDINGS. Acta Pathol Microbiol Scand. 1964;60:36–46. doi: 10.1111/apm.1964.60.1.36. [DOI] [PubMed] [Google Scholar]
  3. BUEHLER E., BODIS I., ROSSIER R., STALDER G. [Trisomy 13-15 with cebocephaly]. Ann Paediatr. 1962;199:198–205. [PubMed] [Google Scholar]
  4. CARR D. H. CHROMOSOME STUDIES IN SPONTANEOUS ABORTIONS. Obstet Gynecol. 1965 Sep;26:308–326. [PubMed] [Google Scholar]
  5. CONEN P. E., ERKMAN B. NECROPSY SPLEEN SAMPLES FOR CHROMOSOME CULTURES. Lancet. 1964 Mar 21;1(7334):665–665. doi: 10.1016/s0140-6736(64)91485-0. [DOI] [PubMed] [Google Scholar]
  6. CONEN P. E., PHILLIPS K. G., MAUNTNER L. S. Multiple developmental anomalies and trisomy of a 13-15 group chromosome ('D' syndrome). Can Med Assoc J. 1962 Sep 29;87:709–712. [PMC free article] [PubMed] [Google Scholar]
  7. Conen P. E., Erkman B. Frequency and occurrence of chromosomal syndromes: II. E-trisomy. Am J Hum Genet. 1966 Jul;18(4):387–398. [PMC free article] [PubMed] [Google Scholar]
  8. Conen P. E., Erkman B., Metaxotou C. The "D" syndrome. Report of four trisomic and one D/D translocation case. Am J Dis Child. 1966 Mar;111(3):236–247. doi: 10.1001/archpedi.1966.02090060046002. [DOI] [PubMed] [Google Scholar]
  9. DEMYER W., ZEMAN W., PALMER C. D. FAMILIAL ALOBAR HOLOPROSENCEPHALY (ARHINENCEPHALY) WITH MEDIAN CLEFT LIP AND PALATE. REPORT OF PATIENT WITH 46 CHROMOSOMES. Neurology. 1963 Nov;13:913–918. doi: 10.1212/wnl.13.11.913. [DOI] [PubMed] [Google Scholar]
  10. Day R. W. The epidemiology of chromosome aberrations. Am J Hum Genet. 1966 Jan;18(1):70–80. [PMC free article] [PubMed] [Google Scholar]
  11. HUEHNS E. R., LUTZNER M., HECHT F. NUCLEAR ABNORMALITIES OF THE NEUTROPHILS IN D1 (13-15)-TRISOMY SYNDROME. Lancet. 1964 Mar 14;1(7333):589–590. doi: 10.1016/s0140-6736(64)91336-4. [DOI] [PubMed] [Google Scholar]
  12. JONGBLOET P., VANWINCKEL H., ANDRIAENSSENS K., HOOFT C. SPORADIC TRISOMY D1 WITH TRANSLOCATION D-D. Helv Paediatr Acta. 1964 Jul;19:121–126. [PubMed] [Google Scholar]
  13. KOENIG E. U., LUBS H. A., Jr, BRANDT I. K. The relationship between congenital anomalies and autosomal chromosome abnormalities. Yale J Biol Med. 1962 Oct;35:189–205. [PMC free article] [PubMed] [Google Scholar]
  14. LUBS H. A., Jr, KOENIG E. U., BRANDT I. K. Trisomy 13-15: a clinical syndrome. Lancet. 1961 Nov 4;2(7210):1001–1002. doi: 10.1016/s0140-6736(61)90963-1. [DOI] [PubMed] [Google Scholar]
  15. MARDEN P. M., SMITH D. W., MCDONALD M. J. CONGENITAL ANOMALIES IN THE NEWBORN INFANT, INCLUDING MINOR VARIATIONS. A STUDY OF 4,412 BABIES BY SURFACE EXAMINATION FOR ANOMALIES AND BUCCAL SMEAR FOR SEX CHROMATIN. J Pediatr. 1964 Mar;64:357–371. doi: 10.1016/s0022-3476(64)80188-8. [DOI] [PubMed] [Google Scholar]
  16. MARIN-PADILLA M., HOEFNAGEL D., BENIRSCHKE K. ANATOMIC AND HISTOPATHOLOGIC STUDY OF TWO CASES OF D1 (13-15) TRISOMY. Cytogenetics. 1964;3:258–284. [PubMed] [Google Scholar]
  17. POWARS D., ROHDE R., GRAVES D. FOETAL HAEMOGLOBIN AND NEUTROPHIL ANOMALY IN THE D1-TRISOMY SYNDROME. Lancet. 1964 Jun 20;1(7347):1363–1364. doi: 10.1016/s0140-6736(64)92043-4. [DOI] [PubMed] [Google Scholar]
  18. PRADER A. [The clinical aspects of common chromosomal abnormalities]. Helv Med Acta. 1962 Dec;29:403–419. [PubMed] [Google Scholar]
  19. ROSENFIELD R. L., BREIBART S., ISAACS H., Jr, KLEVIT H. D., MELLMAN W. J. Trisomy of chromosomes 13-15 and 17-18: its association with infantile arteriosclerosis. Am J Med Sci. 1962 Dec;244:763–779. doi: 10.1097/00000441-196212000-00014. [DOI] [PubMed] [Google Scholar]
  20. SCHAERER K., HAUSCHTECK E., MUEHLETHALER J. P. [Trisomy D syndrome]. Helv Med Acta. 1962 Dec;29:423–424. [PubMed] [Google Scholar]
  21. SERGOVICH F., MADRONICH J. S., BARR M. L., CARR D. H., LANGDON W. A. The D trisomy syndrome: a case report with a description of ocular pathology. Can Med Assoc J. 1963 Jul 27;89:151–157. [PMC free article] [PubMed] [Google Scholar]
  22. SMITH D. W. AUTOSOMAL ABNORMALITIES. Am J Obstet Gynecol. 1964 Dec 1;90:SUPPL–SUPPL:1077. doi: 10.1016/0002-9378(64)90835-x. [DOI] [PubMed] [Google Scholar]
  23. SMITH D. W., PATAU K., THERMAN E., INHORN S. L., DEMARS R. I. The D-I trisomy syndrome. J Pediatr. 1963 Mar;62:326–341. doi: 10.1016/s0022-3476(63)80129-8. [DOI] [PubMed] [Google Scholar]
  24. TAYLOR A. I., POLANI P. E. AUTOSOMAL TRISOMY SYNDROMES, EXCLUDING DOWN'S. Guys Hosp Rep. 1964;113:231–249. [PubMed] [Google Scholar]
  25. TELLER W., PFEIFFER R. A. DIE TRISOMIE D1(13-15) ALS URSACHE MULTIPLER ABARTUNGEN. Z Kinderheilkd. 1964 Feb 14;89:36–48. [PubMed] [Google Scholar]
  26. THERMAN E., PATAU K., SMITH D. W., DEMARS R. I. The D triisomy syndrome and XO gonadal dysgenesis in two sisters. Am J Hum Genet. 1961 Jun;13:193–204. [PMC free article] [PubMed] [Google Scholar]
  27. TOWNES P. L., DEHART G. K., Jr, HECHT F., MANNING J. A. Trisomy 13-15 in a male infant. J Pediatr. 1962 Apr;60:528–532. doi: 10.1016/s0022-3476(62)80113-9. [DOI] [PubMed] [Google Scholar]
  28. UCHIDA I. A., PATAU K., SMITH D. W. Dermal patterns of 18 and D1 trisomics. Am J Hum Genet. 1962 Dec;14:345–352. [PMC free article] [PubMed] [Google Scholar]
  29. WARBURG M., MIKKELSEN M. A CASE OF 13-15 TRISOMY OR BARTHOLIN-PATAU'S SYNDROME. Acta Ophthalmol (Copenh) 1963;41:321–334. doi: 10.1111/j.1755-3768.1963.tb02445.x. [DOI] [PubMed] [Google Scholar]
  30. YUNIS J. J., HOOK E. B., MAYER M. DEOXYRIBONUCLEIC-ACID REPLICATION PATTERN OF TRISOMY D1. Lancet. 1964 Oct 31;2(7366):935–937. doi: 10.1016/s0140-6736(64)90864-5. [DOI] [PubMed] [Google Scholar]

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