Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: Abnormalities and FOXL2[original query] |
---|
Identification of novel mutations in FOXL2 associated with premature ovarian failure. Molecular human reproduction 2002 Aug 8 (8): 729-33. Harris S E, Chand A L, Winship I M, Gersak K, Aittomäki K, Shelling A |
Next Generation Sequencing Should Be Proposed to Every Woman With "Idiopathic" Primary Ovarian Insufficiency. Journal of the Endocrine Society 2021 6 5 (7): bvab032. Eskenazi Sarah, Bachelot Anne, Hugon-Rodin Justine, Plu-Bureau Genevieve, Gompel Anne, Catteau-Jonard Sophie, Molina-Gomes Denise, Dewailly Didier, Dodé Catherine, Christin-Maitre Sophie, Touraine Philip |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 29, 2024
- Content source: