Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Deafness and TMIE[original query] |
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Identification of novel variants in the TMIE gene of patients with nonsyndromic hearing loss. International journal of pediatric otorhinolaryngology 2010 May 74 (5): 489-93. Yang Jiann-Jou, Su Mao-Chang, Chien Kuo-Hsuan, Hsin Chung-Han, Li Shuan-Y |
Comprehensive Analysis of Deafness Genes in Families with Autosomal Recessive Nonsyndromic Hearing Loss. PloS one 2015 10 (11): e0142154. Atik Tahir, Onay Huseyin, Aykut Ayca, Bademci Guney, Kirazli Tayfun, Tekin Mustafa, Ozkinay Fer |
Genetic Aetiology of Nonsyndromic Hearing Loss in Moravia-Silesia. Medicina (Kaunas, Lithuania) 2018 10 54 (2): . Plevova Pavlina, Tvrda Petra, Paprskarova Martina, Turska Petra, Kantorova Barbara, Mrazkova Eva, Zapletalova Ja |
Analysis of TMIE gene mutations including the first large deletion of exon 1 with autosomal recessive non-syndromic deafness. BMC medical genomics 2022 6 15 (1): 133. Rayat Sima, Farhadi Mohammad, Emamdjomeh Hessamaldin, Morovvati Saeid, Falah Masoum |
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- Page last updated:Apr 22, 2024
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