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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: Deafness and meta-analysis and GJB2[original query]
The 35delG mutation in the connexin 26 gene (GJB2) associated with congenital deafness: European carrier frequencies and evidence for its origin in ancient Greece.
Genetic testing 2005 9 (1): 20-5.
Lucotte Gérard, Diéterlen Flore
Prevalence and Characteristics of STRC Gene Mutations (DFNB16): A Systematic Review and Meta-Analysis.
Frontiers in genetics 2021 10 12 707845.
Han Shuang, Zhang Dejun, Guo Yingyuan, Fu Zeming, Guan Guofa
[Meta-analysis for the association of GJB2 gene p.V37I variant and its types with the risk of deafness].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2022 12 39 (12): 1313-1318.
Wang Zaihua, Shao Ying, Li J
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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