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Query Trace: Syndrome and FOXL2[original query]

A novel FOXL2 gene mutation and BMP15 variants in a woman with primary ovarian insufficiency and blepharophimosis-ptosis-epicanthus inversus syndrome. Menopause (New York, N.Y.) 2015 May . Settas Nikolaos, Anapliotou Margarita, Kanavakis Emmanuel, Fryssira Helen, Sofocleous Christalena, Dacou-Voutetakis Catherine, Chrousos George P, Voutetakis Anton Similar articles in PubMed
Mutation analysis of FOXL2 gene in Chinese patients with premature ovarian failure. Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology 2010 Apr 26 (4): 246-9. Ni Feng, Wen Qiaolian, Wang Binbin, Zhou Sirui, Wang Jing, Mu Yuan, Ma Xu, Cao Yunx Similar articles in PubMed
Identification of copy number variants associated with BPES-like phenotypes. Human genetics 2008 Dec 124 (5): 489-98. Gijsbers Antoinet C J, D'haene Barbara, Hilhorst-Hofstee Yvonne, Mannens Marcel, Albrecht Beate, Seidel Joerg, Witt David R, Maisenbacher Melissa K, Loeys Bart, van Essen Ton, Bakker Egbert, Hennekam Raoul, Breuning Martijn H, De Baere Elfride, Ruivenkamp Claudia A Similar articles in PubMed
Mutations in the coding region of the FOXL2 gene are not a major cause of idiopathic premature ovarian failure. Molecular human reproduction 2004 Aug 10 (8): 555-7. Bodega B, Porta C, Crosignani P G, Ginelli E, Marozzi Similar articles in PubMed