Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: Syndrome and LHX1[original query] |
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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 |
Array-comparative genomic hybridization analysis in patients with Müllerian fusion anomalies. Clinical genetics 2017 10 93 (3): 640-646. Ledig S, Tewes A C, Hucke J, Römer T, Kapczuk K, Schippert C, Hillemanns P, Wieacker |
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