Azoospermia related to a unique karyotype: 45,XY,−13,−19,+der(19)t(13;19)(q12;p13)-Reference-Cited by-同舟云学术

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Azoospermia related to a unique karyotype: 45,XY,−13,−19,+der(19)t(13;19)(q12;p13)

Published:2011-03-08 Issue:3 Volume:52 Page:341-344
ISSN:1234-1983
Container-title:Journal of Applied Genetics
language:en
Short-container-title:J Appl Genetics

Author:

Fu Chao,Yun Xin,Dong Yuan,Wu Bai-Yan,Han Rong-Rong,Liu Rui-Zhi

Publisher

Springer Science and Business Media LLC

Subject

Genetics,General Medicine

Link

http://link.springer.com/content/pdf/10.1007/s13353-011-0034-4.pdf

Reference20 articles.

1. Brisset S, Izard V, Misrahi M et al (2005) Cytogenetic, molecular and testicular tissue studies in an infertile 45,X male carrying an unbalanced (Y;22) translocation: case report. Hum Reprod 20(8):2168–2172

2. Diaz-Castaños LR, Rivera H, Gonzalez-Montes RM et al (1991) Translocation (Y;19)(q12;q13) and azoospermia. Ann Génét 34(1):27–29

3. Escudero T, Lee M, Carrel D et al (2000) Analysis of chromosome abnormalities in sperm and embryos from two 45,XY,t(13;14)(q10;q10) carriers. Prenat Diagn 20(7):599–602

4. Ezeh UI, Moore HM (2001) Redefining azoospermia and its implications. Fertil Steril 75(1):213–214

5. Gabriel-Robez O, Ratomponirina C, Dutrillaux B et al (1986) Meiotic association between the XY chromosomes and the autosomal quadrivalent of a reciprocal translocation in two infertile men, 46,XY,t(19;22) and 46,XY,t(17;21). Cytogenet Cell Genet 43(3–4):154–160

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