Associated Papers
Mutations in WNT9B are associated with Mayer-Rokitansky-Küster-Hauser syndrome.
Waschk DE et al.
Clinical Genetics, 2016
Associations of Polymorphisms in WNT9B and PBX1 with Mayer-Rokitansky-Küster-Hauser Syndrome in Chinese Han.
Ma W et al.
Plos One, 2015
WNT9B in 542 Chinese women with Müllerian duct abnormalities: mutation analysis.
Tang R et al.
Reproductive Biomedicine Online, 2014
Analysis of WNT9B mutations in Chinese women with Mayer-Rokitansky-Küster-Hauser syndrome.
Wang M et al.
Reproductive Biomedicine Online, 2014
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