A novel, rapid, and accurate method for detecting microdeletion involving the DAZ gene in infertile men
Author:
Publisher
Elsevier BV
Subject
Obstetrics and Gynecology,Reproductive Medicine
Reference14 articles.
1. Localization of factors controlling spermatogenesis in the nonfluorescent portion of the human Y chromosome;Tiepolo;Hum Genet,1976
2. Diverse spermatogenic defects in humans caused by Y chromosome deletions encompassing a novel RNA-binding protein gene;Reijo;Nat Genet,1995
3. Severe oligozoospermia resulting from deletions of azoospermia factor gene on Y chromosome;Reijo;Lancet,1996
4. Screening for deletions of the Y chromosome involving the DAZ (Deleted in AZoospermia) gene in azoospermia and severe oligozoospermia;Simoni;Fertil Steril,1997
5. The DAZ gene cluster on the human Y chromosome arose from an autosomal gene that was transposed, repeatedly amplified and pruned;Saxena;Nat Genet,1996
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. Clinical data and parenthood of 63 infertile and Y-microdeleted men;Fertility and Sterility;2010-02
2. Loss of the AZFc region due to a human Y-chromosome microdeletion in infertile male patients;Genetics and Molecular Research;2010
3. EVALUATION OF DAZ MICRODELETIONS IN 34 INFERTILE MEN;Archives of Andrology;2006-01
4. Les méthodes de détection des microdélétions du chromosome Y : intérêt d’une nouvelle approche fondée sur la méthode d’électrophorèse en gradient de gel dénaturant;Gynécologie Obstétrique & Fertilité;2003-07
5. Clinical characterization of 42 oligospermic or azoospermic men with microdeletion of the AZFc region of the Y chromosome, and of 18 children conceived via ICSI;Human Reproduction;2002-11-01
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