Associated Papers
FOXL2 mutations lead to different ovarian phenotypes in BPES patients: Case Report.
Méduri G et al.
Human Reproduction (oxford, England), 2010
Identification of 34 novel and 56 known FOXL2 mutations in patients with Blepharophimosis syndrome.
Beysen D et al.
Human Mutation, 2008
Three novel FOXL2 gene mutations in Chinese patients with blepharophimosis-ptosis-epicanthus inversus syndrome.
Or SF et al.
Chinese Medical Journal, 2006
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