Associated Papers
The Persistent Müllerian Duct Syndrome: An Update Based Upon a Personal Experience of 157 Cases.
Picard JY et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation, 2017
Loss-of-function mutations in HOXC13 cause pure hair and nail ectodermal dysplasia.
Lin Z et al.
American Journal of Human Genetics, 2012
Analysis of anti-Müllerian hormone (AMH) and its receptor (AMHR2) genes in patients with persistent Müllerian duct syndrome.
Nishi MY et al.
Arquivos Brasileiros De Endocrinologia E Metabologia, 2012
Natural mutations of the anti-Mullerian hormone type II receptor found in persistent Mullerian duct syndrome affect ligand binding, signal transduction and cellular transport.
Belville C et al.
Human Molecular Genetics, 2009
Surgical management and molecular diagnosis of persistent Müllerian duct syndrome in Chinese patients.
Tian HJ et al.
Asian Journal of Andrology, 0
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