Condition: Mullerian Aplasia and Hyperandrogenism


rs121908650 in WNT4 gene and Mullerian Aplasia and Hyperandrogenism PMID 18182450 2008 Identification and functional analysis of a new WNT4 gene mutation among 28 adolescent girls with primary amenorrhea and müllerian duct abnormalities: a French collaborative study.

PMID 16959810 2007 WNT4 deficiency--a clinical phenotype distinct from the classic Mayer-Rokitansky-Kuster-Hauser syndrome: a case report.

PMID 15317892 2004 A WNT4 mutation associated with Müllerian-duct regression and virilization in a 46,XX woman.

rs121908653 in WNT4;LOC105376845 gene and Mullerian Aplasia and Hyperandrogenism PMID 16959810 2007 WNT4 deficiency--a clinical phenotype distinct from the classic Mayer-Rokitansky-Kuster-Hauser syndrome: a case report.

PMID 18182450 2008 Identification and functional analysis of a new WNT4 gene mutation among 28 adolescent girls with primary amenorrhea and müllerian duct abnormalities: a French collaborative study.

PMID 15317892 2004 A WNT4 mutation associated with Müllerian-duct regression and virilization in a 46,XX woman.