Y-chromosome microdeletion and phenotype in cytogenetically normal men with idiopathic azoospermia
Author:
Publisher
Elsevier BV
Subject
Obstetrics and Gynecology,Reproductive Medicine
Reference22 articles.
1. Diverse spermatogenic defects in humans caused by Y chromosome deletions encompassing a novel RNA-binding protein gene;Reijo;Nat Genet,1995
2. Severe oligospermia resulting from deletions of azoospermia factor gene on Y chromosome;Reijo;Lancet,1996
3. Human Y chromosome azoospermia factors (AZF) mapped to different subregions in Yq11;Vogt;Hum Mol Genet,1996
4. Azoospermic men with deletion of the DAZ gene cluster are capable of completing spermatogenesis;Mulhall;Hum Reprod,1997
5. Y chromosome deletions in azoospermic and severely oligozoospermic men undergoing intracytoplasmic sperm injection after testicular sperm extraction;Silber;Hum Reprod,1998
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