Mutations inWNT9Bare associated with Mayer-Rokitansky-Küster-Hauser syndrome

Variations in RBM8A and TBX6 are associated with disorders of the müllerian ducts

(2015) Ann-Christin Tewes et al.   FERTILITY AND STERILITY

TBX6, LHX1 and copy number variations in the complex genetics of Müllerian aplasia

(2013) Maria Sandbacka et al.   Orphanet Journal of Rare Diseases

WNT9B in 542 Chinese women with Müllerian duct abnormalities: mutation analysis

(2013) Rong Tang et al.   REPRODUCTIVE BIOMEDICINE ONLINE

Frame shift mutation of LHX1 is associated with Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome

(2012) S. Ledig et al.   HUMAN REPRODUCTION

Recurrent aberrations identified by array-CGH in patients with Mayer-Rokitansky-Küster-Hauser syndrome

(2010) Susanne Ledig et al.   FERTILITY AND STERILITY

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

(2008) Pascal Philibert et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM