Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Hearing Loss and meta-analysis and SLC26A4[original query] |
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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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