A case of double aneuploidy, 47,XXY,14-,t(13q14q)+, also probably homozygous for the cystic fibrosis gene.-Reference-Cited by-同舟云学术

A case of double aneuploidy, 47,XXY,14-,t(13q14q)+, also probably homozygous for the cystic fibrosis gene.

Published:1972-06-01 Issue:2 Volume:9 Page:232-235
ISSN:1468-6244
Container-title:Journal of Medical Genetics
language:en
Short-container-title:Journal of Medical Genetics

Author:

Lindenbaum R H,Blackwell N L,De Sa' D J

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference41 articles.

1. Two extra-X chromosomes found in a teen-age girl;Hospital Tribune,1968

2. A female with the 48, XXXX karyotype;Berkeley, M.I.K.; Faed, M.J.W.;Journal of Medical Genetics,1970

3. Syndrome 48, XXXX chez une enfant de six ans. Transmission anormale de groupe Xg;De Grouchy, J.; Brissaud, H.E.; Richardet, J.M.; Repesee, G.; Sanger, R.; Race, R.R.; Salmon, C.; Salmon, D.;Annales de Genetique,1968

4. An XXXX sex chromosome complement in a female with mild mental retardation;Duncan, B.P.; Nicholl, J.A.; Downes, R.;Canadian Medical Association_Journal,1970

5. Rozszczep tqcz6wki u dziewczynki z kariotypem 48, XXXX;Hanicka, M.; Kleczkowska, A.; Makowska, J.; Sokolowski, J.; Jarczyk, K.;Polski Tygodnik Lekarski,1969

Cited by 6 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Concomitance of 47,XXY, a balanced reciprocal translocation of t(4;17)(q12;q11.2) encompassing SPINK2 at 4q12 and NOS at 17q11.2 and an AZFa sY86 deletion in an infertile male;Taiwanese Journal of Obstetrics and Gynecology;2023-03

2. Biochemical and Molecular Genetics of Cystic Fibrosis;Advances in Human Genetics;1991

3. LOCUS FOR CYSTIC FIBROSIS;The Lancet;1984-05

4. A Transferrin Variant in a Kindred with Cystic Fibrosis;Human Heredity;1981

5. Reproductive risk of t(13q14q) carriers: Case report and review;American Journal of Medical Genetics;1979