Associated Papers
Epidermal second-hit mutation in MVK gene associated with linear porokeratosis.
Zhao A et al.
Genes & Diseases, 2025
39386107 (PubMed )
Supplement: mmc2.xlsx › standard
Nonsense mutation of EMX2 is potential causative for uterus didelphysis: first molecular explanation for isolated incomplete müllerian fusion.
Liu S et al.
Fertility and Sterility, 2015
Associations of Polymorphisms in WNT9B and PBX1 with Mayer-Rokitansky-Küster-Hauser Syndrome in Chinese Han.
Ma W et al.
Plos One, 2015
Variants of the WNT7A gene in Chinese patients with müllerian duct abnormalities.
Dang Y et al.
Fertility and Sterility, 2012
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