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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 - 4 (of 4 Records)

Query Trace: Hearing Loss and meta-analysis and SLC26A4[original query]
A systematic review and meta-analysis of common mutations of SLC26A4 gene in Asian populations.
International journal of pediatric otorhinolaryngology 2013 Oct 77 (10): 1670-6.
Du Wan, Guo Yufen, Wang Changlan, Wang Yanli, Liu Xiaow
Diagnostic Value of SLC26A4 Mutation Status in Hereditary Hearing Loss With EVA: A PRISMA-Compliant Meta-Analysis.
Medicine 2015 Dec 94 (50): e2248.
Lu Ya-Jie, Yao Jun, Wei Qin-Jun, Xing Guang-Qian, Cao X
The worldwide frequency of MYO15A gene mutations in patients with non-syndromic hearing loss: A meta-analysis.
Iranian journal of basic medical sciences 2020 8 23 (7): 841-848.
Farjami Mahsa, Assadi Reza, Afzal Javan Fahimeh, Alimardani Malihe, Eslami Saeid, Mansoori Derakhshan Sima, Eslahi Atieh, Mojarrad Maj
Whole Exome Sequencing of Non-Syndromic Hearing Loss Patients.
Iranian journal of public health 2024 6 53 (2): 453-461.
Hossein Naddafnia, Zahra Noormohammadi, Shiva Irani, Iman Salahshoorif
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