Analysis of WNT9B mutations in Chinese women with Mayer–Rokitansky–Küster–Hauser syndrome

Wnt9b Plays a Central Role in the Regulation of Mesenchymal to Epithelial Transitions Underlying Organogenesis of the Mammalian Urogenital System

Thomas J. Carroll, Joo-Seop Park, Shigemi Hayashi et al. · Developmental Cell · 2005 · 903 citations · Full text

Life Sciences, Developmental Biology, Molecular Biology +15

Cellular mechanisms of Müllerian duct formation in the mouse

Grant D. Orvis, Richard R. Behringer · Developmental Biology · 2007 · 219 citations · Full text

Life Sciences, Cell Biology, Developmental Biology +11

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

Susanne Ledig, Cordula Schippert, Reiner Strick et al. · Fertility and Sterility · 2010 · 133 citations · Full text

Life Sciences, Oncology, Human Genetics +4

<i>Wnt9b</i> is the mutated gene involved in multifactorial nonsyndromic cleft lip with or without cleft palate in A/WySn mice, as confirmed by a genetic complementation test

D. M. Juriloff, Muriel J. Harris, Andrew P. McMahon et al. · Birth Defects Research Part A Clinical and Molecular Teratology · 2006 · 127 citations

Dentistry, Genetics, Molecular Genetics +17

High incidence of recurrent copy number variants in patients with isolated and syndromic Müllerian aplasia

Serena Nik‐Zainal, Reiner Strick, Mekayla A. Storer et al. · Journal of Medical Genetics · 2011 · 122 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17