Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Deafness and MYH9[original query] |
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Identification of six novel MYH9 mutations and genotype-phenotype relationships in autosomal dominant macrothrombocytopenia with leukocyte inclusions. Journal of human genetics 2002 1 46 (12): 722-9. Kunishima S, Matsushita T, Kojima T, Amemiya N, Choi Y M, Hosaka N, Inoue M, Jung Y, Mamiya S, Matsumoto K, Miyajima Y, Zhang G, Ruan C, Saito K, Song K S, Yoon H J, Kamiya T, Saito |
Mutations in MYH9 exons 1, 16, 26, and 30 are infrequently found in Japanese patients with nonsyndromic deafness. Genetic testing and molecular biomarkers 2009 Oct 13 (5): 705-7. Kunishima Shinji, Matsunaga Tatsuo, Ito Yoshimi, Saito Hidehi |
Progressive macrothrombocytopenia and hearing loss in a large family with DIAPH1 related disease. American journal of medical genetics. Part A 2017 8 173 (10): 2826-2830. Ganaha Akira, Kaname Tadashi, Shinjou Ayano, Chinen Yasutsugu, Yanagi Kumiko, Higa Teruyuki, Kondo Shunsuke, Suzuki Mik |
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