Human Genome Epidemiology Literature Finder
Records 1 - 8 (of 8 Records) |
Query Trace: Hearing and MYH9[original query] |
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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 |
Nonmuscle Myosin Heavy Chain IIA Mutation Predicts Severity and Progression of Sensorineural Hearing Loss in Patients With MYH9-Related Disease. Ear and hearing 2015 Jul . Verver Eva J J, Topsakal Vedat, Kunst Henricus P M, Huygen Patrick L M, Heller Paula G, Pujol-Moix Nuria, Savoia Anna, Benazzo Marco, Fierro Tiziana, Grolman Wilko, Gresele Paolo, Pecci Alessand |
Genetic association of MYH genes with hereditary hearing loss in Korea. Gene 2016 Jul . Kim Sang-Joo, Lee Seokwon, Park Hong-Joon, Kang Tae-Hun, Sagong Borum, Baek Jeong-In, Oh Se-Kyung, Choi Jae Young, Lee Kyu-Yup, Kim Un-Kyu |
Late onset and high-frequency dominant hearing loss in a family with MYH9 disorder. European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery 2016 Mar . Wasano Koichiro, Matsunaga Tatsuo, Ogawa Kaoru, Kunishima Shin |
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 |
A Genomic and Protein-Protein Interaction Analyses of Nonsyndromic Hearing Impairment in Cameroon Using Targeted Genomic Enrichment and Massively Parallel Sequencing. Omics : a journal of integrative biology 2017 1 21 (2): 90-99. Lebeko Kamogelo, Manyisa Noluthando, Chimusa Emile R, Mulder Nicola, Dandara Collet, Wonkam Ambroi |
Genetic Inheritance of Late-Onset, Down-Sloping Hearing Loss and Its Implications for Auditory Rehabilitation. Ear and hearing 2019 5 41 (1): 114-124. Song Mee Hyun, Jung Jinsei, Rim John Hoon, Choi Hye Ji, Lee Hack June, Noh Byunghwa, Lee Jun Suk, Gee Heon Yung, Choi Jae You |
MYH9 disorder: Identification and a novel mutation in patients with macrothrombocytopenia. Pediatric blood & cancer 2021 4 68 (7): e29055. Natesirinilkul Rungrote, Sosothikul Darintr, Komwilaisak Patcharee, Pongtanakul Bunchoo, Narkbunnum Nattee, Yudhasompop Najwa, Mekjarusgool Pimsiri, Niparuck Pimjai, Boonyawat Kochawan, Kunishima Shinji, Sirachainan Nongnuch, |
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- Page last updated:Apr 16, 2024
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