Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 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 |
Genetic diagnosis of childhood sensorineural hearing loss. Acta otorrinolaringologica espanola 2024 1 . Sara Reda Del Barrio, Alfredo García Fernández, Juan Francisco Quesada-Espinosa, María Teresa Sánchez-Calvín, Irene Gómez-Manjón, Olalla Sierra-Tomillo, Alexandra Juárez-Rufián, Joaquín de Vergas Gutiérr |
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