Article
Associations of Polymorphisms in WNT9B and PBX1 with Mayer-Rokitansky-Küster-Hauser Syndrome in Chinese Han.
PloS one - 1 Jan 2015
Ma Wenqing, Li Ya, Wang Man, Li Haixia, Su Tiefen, Li Yan, Wang Shixuan
Abstract excerpt
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 investigated whether these reported variants are associated with MRKH syndrome (types I and II) in a relatively large sample...
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