Skip to main content
Journal of Medical Genetics logoLink to Journal of Medical Genetics
. 1970 Jun;7(2):177–179. doi: 10.1136/jmg.7.2.177

Familial occurrence of congenital malformations and ring chromosome (46,XX,Cr).

G Gacs, D Schuler, M Sellyei
PMCID: PMC1468810  PMID: 5534843

Full text

PDF
177

Images in this article

Selected References

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

  1. Atkins L., Pant S. S., Hazard G. W., Ouellette E. M. Two cases with a C-group ring autosome. Ann Hum Genet. 1966 Jul;30(1):1–6. doi: 10.1111/j.1469-1809.1966.tb00001.x. [DOI] [PubMed] [Google Scholar]
  2. Butler L. J., France N. E., Jacoby N. M. An infant with multiple congenital anomalies and a ring chromosome in group C (X-6-12). J Med Genet. 1967 Dec;4(4):295–298. doi: 10.1136/jmg.4.4.295. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. 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]
  4. Schuler D. Ujabb módszerek az emberi chromosoma vizsgálatára. Orv Hetil. 1965 Dec 12;106(50):2366–2367. [PubMed] [Google Scholar]
  5. TURNER B., JENNINGS A. N., den DULK G. M., STAPLETON T. A self-perpetuating ring chromosome. Med J Aust. 1962 Jul 14;49(2):56–58. [PubMed] [Google Scholar]

Articles from Journal of Medical Genetics are provided here courtesy of BMJ Publishing Group

RESOURCES