Screening for deletions of the Y chromosome involving the DAZ (Deleted in AZoospermia) gene in azoospermia and severe oligozoospermia-Reference-Cited by-同舟云学术

Screening for deletions of the Y chromosome involving the DAZ (Deleted in AZoospermia) gene in azoospermia and severe oligozoospermia

Published:1997-03 Issue:3 Volume:67 Page:542-547
ISSN:0015-0282
Container-title:Fertility and Sterility
language:en
Short-container-title:Fertility and Sterility

Author:

Simoni Manuela,Gromoll Jörg,Dworniczak Bernd,Rolf Claus,Abshagen Katrin,Kamischke Axel,Carani Cesare,Meschede Dieter,Behre Hermann M.,Horst Jürgen,Nieschlag Eberhard

Publisher

Elsevier BV

Subject

Obstetrics and Gynaecology,Reproductive Medicine

Reference25 articles.

1. Localization of factors controlling spermatogenesis in the nonfluorescent portion of the human Y chromosome;Tiepolo;Hum Genet,1976

2. Molecular scanning of Yq11 (interval 6) in men with Sertoli-cellonly syndrome;Johnson;Am J Obstet Gynecol,1989

3. Towards the molecular localization of the AZF locus: mapping of microdeletions in azoospermic men within 14 subintervals of interval 6 of the human Y chromosome;Ma;Hum Mol Genet,1992

4. A Y chromosome gene family with RNA-binding protein homology: candidates for the azoospermia factor AZF controlling human spermatogenesis;Ma;Cell,1993

5. Microdeletions in interval 6 of the Y chromosome of males with idiopathic sterility point to disruption of AZF, a human spermatogenesis gene;Vogt;Hum Genet,1992

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