Human Genome Epidemiology Literature Finder
Records 1 - 7 (of 7 Records) |
Query Trace: TMIE[original query] |
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Novel sequence variants in the TMIE gene in families with autosomal recessive nonsyndromic hearing impairment. Journal of molecular medicine (Berlin, Germany) 2006 1 84 (3): 226-31. Santos Regie Lyn P, El-Shanti Hatem, Sikandar Shaheen, Lee Kwanghyuk, Bhatti Attya, Yan Kai, Chahrour Maria H, McArthur Nathan, Pham Thanh L, Mahasneh Amjad Abdullah, Ahmad Wasim, Leal Suzanne |
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 |
Evaluating the role of rare genetic variation in sleep duration. Sleep health 2022 7 8 (5): 536-541. Meng Peilin, Pan Chuyu, Cheng Shiqiang, Li Chun'e, Yao Yao, Liu Li, Cheng Bolun, Yang Xuena, Zhang Zhen, Chen Yujing, Zhang Jingxi, Zhang Huijie, Wen Yan, Jia Yumeng, Guo Xiong, Zhang Fe |
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 |
Whole-Exome Sequencing Targeting a Gene Panel for Sensorineural Hearing Loss: The First Portuguese Cohort Study. Cytogenetic and genome research 2022 5 162 (1-2): 1-9. Reis Cláudia Sousa, Quental Sofia, Fernandes Susana, Castedo Sérgio, Moura Carla Pin |
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- Page last updated:Apr 16, 2024
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