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A new FOXL2 gene mutation in a woman with premature ovarian failure and sporadic blepharophimosis-ptosis-epicanthus inversus syndrome
Authors:Frederico José   Silva Corrê  a,Adriano Bueno Tavares,Rinaldo Wellerson Pereira,Mauricio Simõ  es Abrã  o
Affiliation:a Department of Obstetrics and Gynecology, Catholic University of Brasilia, Brasília Federal District, Brazil
b Department of Postgraduate Genomic Science and Biotechnology, Catholic University of Brasília, Brasília Federal District, Brazil
c Department of Gynecology, São Paulo University, São Paulo, São Paulo, Brazil
Abstract:
Keywords:Blepharophimosis-ptosis-epicanthus inversus syndrome   hypergonadotropic hypogonadism   premature ovarian failure   FOXL2 gene   gene mutation
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