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4. Mutations of the AMH type II receptor in two extended families with persistent Müllerian duct syndrome: lack of phenotype/genotype correlation. Abduljabbar M; Taheini K; Picard JY; Cate RL; Josso N Horm Res Paediatr; 2012; 77(5):291-7. PubMed ID: 22584735 [TBL] [Abstract][Full Text] [Related]
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