Mutations in the coding region of the FOXL2 gene are not a major cause of idiopathic premature ovarian failure
Author:
Publisher
Oxford University Press (OUP)
Subject
Cell Biology,Developmental Biology,Obstetrics and Gynecology,Genetics,Molecular Biology,Embryology,Reproductive Medicine
Link
http://academic.oup.com/molehr/article-pdf/10/8/555/3444748/gah078.pdf
Cited by 34 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. Benign Conditions of the Ovary;Diagnostic Gynecologic and Obstetric Pathology;2018
2. Genetics of primary ovarian insufficiency;Clinical Genetics;2016-12-12
3. Primary ovarian insufficiency associated with autosomal abnormalities: from chromosome to genome-wide and beyond;Menopause;2016-07
4. Building Dimorphic Forms;Principles of Developmental Genetics;2015
5. Ethnic specificity of variants of the ESR1, HK3, BRSK1 genes and the 8q22.3 locus: No association with premature ovarian failure (POF) in Serbian women;Maturitas;2014-01
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