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Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- 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]
- CRAWFURD M. D. Multiple congenital anomaly associated with an extra autosome. Lancet. 1961 Jul 1;2(7192):22–24. doi: 10.1016/s0140-6736(61)92709-x. [DOI] [PubMed] [Google Scholar]
- EDWARDS J. H., HARNDEN D. G., CAMERON A. H., CROSSE V. M., WOLFF O. H. A new trisomic syndrome. Lancet. 1960 Apr 9;1(7128):787–790. doi: 10.1016/s0140-6736(60)90675-9. [DOI] [PubMed] [Google Scholar]
- FRACCARO M., KAIJSER K., LINDSTEN J. Chromosomal abnormalities in father and Mongol child. Lancet. 1960 Apr 2;1(7127):724–727. doi: 10.1016/s0140-6736(60)90615-2. [DOI] [PubMed] [Google Scholar]
- FRASER J. H., CAMPBELL J., MACGILLIVRAY R. C., BOYD E., LENNOX B. The XXX syndrome frequency among mental defectives and fertility. Lancet. 1960 Sep 17;2(7151):626–627. doi: 10.1016/s0140-6736(60)91696-2. [DOI] [PubMed] [Google Scholar]
- HAYWARD M. D., BOWER B. D. Chromosomal trisomy associated with the Sturge-Weber syndrome. Lancet. 1960 Oct 15;2(7155):844–846. doi: 10.1016/s0140-6736(60)91908-5. [DOI] [PubMed] [Google Scholar]
- JACOBS P. A., HARNDEN D. G., COURT BROWN W. M., GOLDSTEIN J., CLOSE H. G., MACGREGOR T. N., MACLEAN N., STRONG J. A. Abnormalities involving the X chromosome in women. Lancet. 1960 Jun 4;1(7136):1213–1216. doi: 10.1016/s0140-6736(60)91097-7. [DOI] [PubMed] [Google Scholar]
- 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]
- MACLEAN N., MITCHELL J. M. A survey of sex-chromosome abnormalities among 4514 mental defectives. Lancet. 1962 Feb 10;1(7224):293–296. doi: 10.1016/s0140-6736(62)91244-8. [DOI] [PubMed] [Google Scholar]
- MOORHEAD P. S., NOWELL P. C., MELLMAN W. J., BATTIPS D. M., HUNGERFORD D. A. Chromosome preparations of leukocytes cultured from human peripheral blood. Exp Cell Res. 1960 Sep;20:613–616. doi: 10.1016/0014-4827(60)90138-5. [DOI] [PubMed] [Google Scholar]
- NORTHCUTT R. C. Multiple congenital anomalies in a Negro infant with 13-15 trisomy. South Med J. 1962 Apr;55:385–389. doi: 10.1097/00007611-196204000-00011. [DOI] [PubMed] [Google Scholar]
- PATAU K., SMITH D. W., THERMAN E., INHORN S. L., WAGNER H. P. Multiple congenital anomaly caused by an extra autosome. Lancet. 1960 Apr 9;1(7128):790–793. doi: 10.1016/s0140-6736(60)90676-0. [DOI] [PubMed] [Google Scholar]
- PATAU K., THERMAN E., SMITH D. W., INHORN S. L., PICKEN B. F. Partial-trisomy syndromes. I. Sturge-Weber's disease. Am J Hum Genet. 1961 Sep;13:287–298. [PMC free article] [PubMed] [Google Scholar]
- PENROSE L. S. Mongolism. Br Med Bull. 1961 Sep;17:184–189. doi: 10.1093/oxfordjournals.bmb.a069906. [DOI] [PubMed] [Google Scholar]
- POLANI P. E., BRIGGS J. H., FORD C. E., CLARKE C. M., BERG J. M. A Mongol girl with 46 chromosomes. Lancet. 1960 Apr 2;1(7127):721–724. doi: 10.1016/s0140-6736(60)90614-0. [DOI] [PubMed] [Google Scholar]
- ROWE R. D., UCHIDA I. A. Cardiac malformation in mongolism: a prospective study of 184 mongoloid children. Am J Med. 1961 Nov;31:726–735. doi: 10.1016/0002-9343(61)90157-7. [DOI] [PubMed] [Google Scholar]
- SANDBERG A. A., KOEPF G. F., ISHIHARA T., HAUSCHKA T. S. An XYY human male. Lancet. 1961 Aug 26;2(7200):488–489. doi: 10.1016/s0140-6736(61)92459-x. [DOI] [PubMed] [Google Scholar]
- SMITH D. W., PATAU K., THERMAN E., INHORN S. L. A new autosomal trisomy syndrome: multiple congenital anomalies caused by an extra chromosome. J Pediatr. 1960 Sep;57:338–345. doi: 10.1016/s0022-3476(60)80241-7. [DOI] [PubMed] [Google Scholar]
- SMITH D. W., PATAU K., THERMAN E., INHORN S. L. The No. 18 trisomy syndrome. J Pediatr. 1962 Apr;60:513–527. doi: 10.1016/s0022-3476(62)80112-7. [DOI] [PubMed] [Google Scholar]
- 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]
- 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]
- UCHIDA I. A., BOWMAN J. M., WANG H. C. The 18-trisomy syndrome. N Engl J Med. 1962 Jun 7;266:1198–1201. doi: 10.1056/NEJM196206072662304. [DOI] [PubMed] [Google Scholar]
- UCHIDA I. A., LEWIS A. J., BOWMAN J. M., WANG H. C. A case of double trisomy: trisomy No. 18 and triplo- X. J Pediatr. 1962 Apr;60:498–502. doi: 10.1016/s0022-3476(62)80110-3. [DOI] [PubMed] [Google Scholar]
- ZELLWEGER H., MIKAMO K. Autosomal cytogenetics. Helv Paediatr Acta. 1961 Dec;16:670–690. [PubMed] [Google Scholar]