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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 3 (of 3 Records)

Query Trace: Hearing and RDX[original query]
Genetic causes of nonsyndromic hearing loss in Iran in comparison with other populations.
Journal of human genetics 2010 Oct 55 (10): 639-48.
Mahdieh Nejat, Rabbani Bahareh, Wiley Susan, Akbari Mohammad Taghi, Zeinali Siro
A Genomic and Protein-Protein Interaction Analyses of Nonsyndromic Hearing Impairment in Cameroon Using Targeted Genomic Enrichment and Massively Parallel Sequencing.
Omics : a journal of integrative biology 2017 1 21 (2): 90-99.
Lebeko Kamogelo, Manyisa Noluthando, Chimusa Emile R, Mulder Nicola, Dandara Collet, Wonkam Ambroi
[Mutational analysis of 117 patients with non-syndromic hearing loss].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2019 2 36 (2): 108-111.
Wang Leilei, Gu Ying, Yang Shuting, Mao Huafen, Tang Xinxin, Xu Tianlong, Wu Min, Sun Yuhua, Luo Xiuc
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