Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Goiter and GJB2[original query] |
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Mutation spectrum and genotype-phenotype correlation of hearing loss patients caused by SLC26A4 mutations in the Japanese: a large cohort study. Journal of human genetics 2014 May 59 (5): 262-8. Miyagawa Maiko, Nishio Shin-Ya, Usami Shin-Ichi, |
Novel pathogenic variants underlie SLC26A4-related hearing loss in a multiethnic cohort. International journal of pediatric otorhinolaryngology 2017 10 101 167-171. Cengiz Filiz Basak, Yilmazer Rasim, Olgun Levent, Sennaroglu Levent, Kirazli Tayfun, Alper Hudaver, Olgun Yuksel, Incesulu Armagan, Atik Tahir, Huesca-Hernandez Fabiola, Domínguez-Aburto Juan, González-Rosado Garly, Hernandez-Zamora Edgar, Arenas-Sordo Maria de la Luz, Menendez Ibis, Orhan Kadir Serkan, Avci Hakan, Mahdieh Nejat, Bonyadi Mortaza, Foster Joseph, Duman Duygu, Ozkinay Ferda, Blanton Susan H, Bademci Guney, Tekin Musta |
[Results of molecular genetic testing in Russian patients with Pendred syndrome and allelic disorders]. Genetika 2017 Jan 53 (1): 88-99. Mironovich O L, Bliznetz E A, Markova T G, Geptner E N, Lalayants M R, Zelikovich E I, Tavartkiladze G A, Polyakov A |
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