Mutations of the AMH Type II Receptor in Two Extended Families with Persistent Müllerian Duct Syndrome: Lack of Phenotype/Genotype Correlation-Reference-Cited by-同舟云学术

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Mutations of the AMH Type II Receptor in Two Extended Families with Persistent Müllerian Duct Syndrome: Lack of Phenotype/Genotype Correlation

Published:2012 Issue:5 Volume:77 Page:291-297
ISSN:1663-2826
Container-title:Hormone Research in Paediatrics
language:en
Short-container-title:Horm Res Paediatr

Author:

Abduljabbar Mohammad,Taheini Khalid,Picard Jean-Yves,Cate Richard L.,Josso Nathalie

Publisher

S. Karger AG

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism,Pediatrics, Perinatology, and Child Health

Cited by 30 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Biomedical Perspectives of Herbal Honey;Biomedical Perspectives of Herbal Honey;2024

2. The Persistent Müllerian Duct Syndrome;Genetic Steroid Disorders;2023

3. The Role of the Environment in Testicular Dysgenesis Syndrome;Endocrinology;2023

4. The Role of the Environment in Testicular Dysgenesis Syndrome;Endocrinology;2023

5. Surgical management and molecular diagnosis of persistent Müllerian duct syndrome in Chinese patients;Asian Journal of Andrology;2022

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