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See Latest ArticlesFOXL2 mutations lead to different ovarian phenotypes in BPES patients: Case Report
Human Reproduction, 10/13/09
Touraine P et al. – FOXL2 mutations cause the autosomal dominant Blepharophimosis–ptosis–epicanthus inversus syndrome (BPES) that may be associated with premature ovarian failure (POF). However, little is known about the molecular mechanisms of FOXL2 actions in the human ovary.
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Unexplained fetal loss: the fetal side of thrombophilia
Fertility and Sterility, 11/12/09
Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers
Human Molecular Genetics, 11/03/09
Genetic Variation in the Progesterone Receptor and Metabolism Pathways and Hormone Therapy in Relation to Breast Cancer Risk
American Journal of Epidemiology, 10/22/09
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