Diverse spermatogenic defects in humans caused by Y chromosome deletions encompassing a novel RNA–binding protein gene-Reference-Cited by-同舟云学术

Diverse spermatogenic defects in humans caused by Y chromosome deletions encompassing a novel RNA–binding protein gene

Published:1995-08 Issue:4 Volume:10 Page:383-393
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Reijo Renee,Lee Tien-Yi,Salo Pia,Alagappan Raaji,Brown Laura G.,Rosenberg Michael,Rozen Steve,Jaffe Tom,Straus Donald,Hovatta Outi,de la Chapelle Albert,Silber Sherman,Page David C.

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng0895-383.pdf

Reference43 articles.

1. Clermont, Y. Renewal of spermatogonia in man. Am. J. Anat. 118, 509–524 (1966).

2. Dym, M. Spermatogonial stem cells of the testis. Proc. natn. Acad. Sci. U.S.A. 91, 11287–11289 (1994).

3. Hull, M.G.R. et al. Population study of causes, treatment, and outcome of infertility. Brit. med. J. 291, 1693–1697 (1985).

4. Silber, S.J. The relationship of abnormal semen parameters to male fertility. Hum. Reprod. 4, 947–953 (1989).

5. Tiepolo, L. & Zuffardi, O. Localization of factors controlling spermatogenesis in the nonfluorescent portion of the human Y chromosome long arm. Hum. Genet. 34, 119–124 (1976).

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