Associations of Polymorphisms in WNT9B and PBX1 with Mayer-Rokitansky-Küster-Hauser Syndrome in Chinese Han

BACKGROUND: Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is a rare syndrome that is characterized by congenital aplasia of the uterus and the upper portion (2/3) of the vagina. Previous attempts to identify causal mutations of MRKH syndrome have primarily resulted in negative outcomes. We investig...

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Detalles Bibliográficos
Autores principales: Ma, Wenqing, Li, Ya, Wang, Man, Li, Haixia, Su, Tiefen, Li, Yan, Wang, Shixuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4468103/
https://www.ncbi.nlm.nih.gov/pubmed/26075712
http://dx.doi.org/10.1371/journal.pone.0130202

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