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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 3 (of 3 Records)

Query Trace: Disease and WNT9B[original query]
Mutations in WNT9B are associated with Mayer-Rokitansky-Küster-Hauser syndrome.
Clinical genetics 2015 Nov .
Waschk Daniel E J, Tewes Ann-Christin, Römer Thomas, Hucke Jürgen, Kapczuk Karina, Schippert Cordula, Hillemanns Peter, Wieacker Peter, Ledig Susan
Genetic Variation in WNT9B Increases Relapse Hazard in Multiple Sclerosis. GWAS Catalog
Annals of neurology 2021 3 89 (5): 884-894.
Vandebergh Marijne, Andlauer Till F M, Zhou Yuan, Mallants Klara, Held Friederike, Aly Lilian, Taylor Bruce V, Hemmer Bernhard, Dubois Bénédicte, Goris
Disorders of Sex Development in Individuals Harbouring MAMLD1 Variants: WES and Interactome Evidence of Oligogenic Inheritance.
Frontiers in endocrinology 2021 1 11 582516.
Li Lele, Gao Fenqi, Fan Lijun, Su Chang, Liang Xuejun, Gong ChunX
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