Human Genome Epidemiology Literature Finder
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Records 1 - 4 (of 4 Records) |
| Query Trace: Awareness and GJB2[original query] |
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| Simultaneous screening of multiple mutations by invader assay improves molecular diagnosis of hereditary hearing loss: a multicenter study. PloS one 2012 7 (2): e31276. Usami Shin-ichi, Nishio Shin-ya, Nagano Makoto, Abe Satoko, Yamaguchi Toshikazu, |
| GJB2 and mitochondrial 12S rRNA susceptibility mutations in sudden deafness. 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 2015 Jun . Chen Kaitian, Sun Liang, Zong Ling, Wu Xuan, Zhan Yuan, Dong Chang, Cao Hui, Tang Haocheng, Jiang Hongy |
| [Twenty years of clinical studies of GJB2-linked hearing loss in Russia]. Vestnik otorinolaringologii 2018 8 83 (4): 31-36. Markova T G, Bliznetz E A, Polyakov A V, Tavartkiladze G |
| Comprehensive Study of Germline Mutations and Double-Hit Events in Esophageal Squamous Cell Cancer. Frontiers in oncology 2021 11 637431. Zeng Bing, Huang Peide, Du Peina, Sun Xiaohui, Huang Xuanlin, Fang Xiaodong, Li L |
- Page last reviewed:Feb 1, 2023
- Page last updated:Sep 25, 2023
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