No evidence of the inactivating mutation (C566T) in the follicle-stimulating hormone receptor gene in Brazilian women with premature ovarian failure-Reference-Cited by-同舟云学术

No evidence of the inactivating mutation (C566T) in the follicle-stimulating hormone receptor gene in Brazilian women with premature ovarian failure

Published:1998-09 Issue:3 Volume:70 Page:565-567
ISSN:0015-0282
Container-title:Fertility and Sterility
language:en
Short-container-title:Fertility and Sterility

Author:

da Fonte Kohek Maria Beatriz,Batista Marcelo Cidade,Russell Alan J,Vass Keith,Giacaglia Luciano Ricardo,Mendonca Berenice Bilharinho,Latronico Ana Claudia

Publisher

Elsevier BV

Subject

Obstetrics and Gynecology,Reproductive Medicine

Reference4 articles.

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

2. Clinical features of primary ovarian failure caused by point mutation in the follicle-stimulating hormone receptor gene;Aittomäki;J Clin Endocrinol Metab,1996

3. The follicle-stimulating hormone receptor gene is polymorphic in premature ovarian failure and normal controls;Whitney;Fertil Steril,1995

4. The follicle-stimulating hormone receptor;Simoni;Endocr Rev,1997

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