Novel variants in the SOHLH2 gene are implicated in human premature ovarian failure-Reference-Cited by-同舟云学术

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Novel variants in the SOHLH2 gene are implicated in human premature ovarian failure

Published:2014-04 Issue:4 Volume:101 Page:1104-1109.e6
ISSN:0015-0282
Container-title:Fertility and Sterility
language:en
Short-container-title:Fertility and Sterility

Author:

Qin Yingying,Jiao Xue,Dalgleish Raymond,Vujovic Svetlana,Li Jin,Simpson Joe Leigh,Al-Azzawi Farook,Chen Zi-Jiang

Publisher

Elsevier BV

Subject

Obstetrics and Gynecology,Reproductive Medicine

Reference26 articles.

1. Incidence of premature ovarian failure;Coulam;Obstet Gynecol,1986

2. Primary ovarian insufficiency: a more accurate term for premature ovarian failure;Welt;Clin Endocrinol (Oxf),2008

3. Cytogenetic analysis of 531 Chinese women with premature ovarian failure;Jiao;Hum Reprod,2012

4. The FMR1 premutation and reproduction;Wittenberger;Fertil Steril,2007

5. Mutation in the follicle-stimulating hormone receptor gene causes hereditary hypergonadotropic ovarian failure;Aittomäki;Cell,1995

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