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13. 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. Raile K; Stobbe H; Tröbs RB; Kiess W; Pfäffle R Eur J Endocrinol; 2005 Sep; 153(3):353-8. PubMed ID: 16131596 [TBL] [Abstract][Full Text] [Related]
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