Analysis of FOXO3 mutation in 114 Chinese women with premature ovarian failure
Author:
Publisher
Elsevier BV
Subject
Developmental Biology,Reproductive Medicine,Obstetrics and Gynaecology
Reference25 articles.
1. Mutation in the follicle-stimulating hormone receptor gene causes hereditary hypergonadotropic ovarian failure;Aittomaeki;Cell,1995
2. A human homologue of the Drosophila melanogaster diaphanous gene is disrupted in a patient with premature ovarian failure: evidence for conserved function in oogenesis and implications for human sterility;Bione;Am. J. Hum. Genet.,1998
3. Identification of differing etiologies of clinically diagnosed premature menopause;Board;Am. J. Obstet. Gynecol.,1979
4. Suppression of ovarian follicle activation in mice by the transcription factor Foxo3a;Castrillon;Science,2003
5. Incidence of premature ovarian failure;Coulam;Obstet. Gynecol.,1986
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