A new heterozygous mutation of the FOXL2 gene is associated with a large ovarian cyst and ovarian dysfunction in an adolescent girl with blepharophimosis/ptosis/epicanthus inversus syndrome in: European Journal of Endocrinology Volume 153 Issue 3 (2005)

A new heterozygous mutation of the FOXL2 gene is associated with a large ovarian cyst and ovarian dysfunction in an adolescent girl with blepharophimosis/ptosis/epicanthus inversus syndrome in: European Journal of Endocrinology Volume 153 Issue 3 (2005)

A new heterozygous mutation of the FOXL2 gene is associated with a large ovarian cyst and ovarian dysfunction in an adolescent girl with blepharophimosis/ptosis/epicanthus inversus syndrome

in European Journal of Endocrinology

Authors: K Raile 1 , H Stobbe 1 , R B Tröbs 1 , W Kiess 1 , a