Surgical management and molecular diagnosis of persistent Müllerian duct syndrome in Chinese patients

Persistent Müllerian duct syndrome (PMDS) is a rare clinically and genetically overlapping disorder caused by mutations in the anti-Müllerian hormone (AMH) gene or the anti-Müllerian hormone receptor type 2 (AMHR2) gene. Affected individuals present uterus and tubes in normally virilized males and a...

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Detalles Bibliográficos
Autores principales: Tian, Hong-Juan, Wu, De-Hua, Ru, Wei, Wu, Ding-Wen, Tao, Chang, Chen, Guang-Jie, Yuan, Jin-Na, Fu, Jun-Fen, Tang, Da-Xing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2021
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8788598/
https://www.ncbi.nlm.nih.gov/pubmed/34810374
http://dx.doi.org/10.4103/aja202175

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8788598/
https://www.ncbi.nlm.nih.gov/pubmed/34810374
http://dx.doi.org/10.4103/aja202175

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