Human Genome Epidemiology Literature Finder
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Records 1 - 5 (of 5 Records) |
| Query Trace: Disease and GJB3[original query] |
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| Lack of association between Connexin 31 (GJB3) alterations and sensorineural deafness in Austria. Hearing research 2004 Aug 194 (1-2): 81-6. Frei Klemens, Ramsebner Reinhard, Hamader Gertrude, Lucas Trevor, Schoefer Christian, Baumgartner Wolf-Dieter, Wachtler Franz J, Kirschhofer Kar |
| GJB2 mutations in patients with nonsyndromic hearing loss from Croatia. Genetic testing and molecular biomarkers 2009 Oct 13 (5): 693-9. Sansovi? Ivona, Knezevi? Jelena, Musani Vesna, Seeman Pavel, Barisi? Ingeborg, Paveli? Jasmin |
| Connexin Genes Variants Associated with Non-Syndromic Hearing Impairment: A Systematic Review of the Global Burden. Life (Basel, Switzerland) 2020 10 10 (11): . Adadey Samuel Mawuli, Wonkam-Tingang Edmond, Twumasi Aboagye Elvis, Nayo-Gyan Daniel Wonder, Boatemaa Ansong Maame, Quaye Osbourne, Awandare Gordon A, Wonkam Ambroi |
| Genetic Susceptibility Study of Chinese Sudden Sensorineural Hearing Loss Patients with Vertigo. Current medical science 2021 Aug 41 (4): 673-679. Gao Yun, Wang Hong-Yang, Guan Jing, Lan Lan, Zhao Cui, Xie Lin-Yi, Wang Da-Yong, Wang Qiu- |
| [A prospective study of genetic screening of 2 060 neonates by high-throughput sequencing]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2023 5 40 (6): 641-647. Danyan Zhuang, Fei Wang, Shuxia Ding, Zhoushu Zheng, Qi Yu, Lanqiu Lyu, Shuni Sun, Rulai Yang, Wenwen Que, Haibo |
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