Human Genome Epidemiology Literature Finder
Records 1 - 6 (of 6 Records) |
Query Trace: Deafness and POU4F3[original query] |
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Targeted genomic capture and massively parallel sequencing to identify novel variants causing Chinese hereditary hearing loss. Journal of translational medicine 2014 12 (1): 311. Wei Qinjun, Zhu Hongmei, Qian Xuli, Chen Zhibin, Yao Jun, Lu Yajie, Cao Xin, Xing Guangqi |
Mutation in the Hair Cell Specific Gene POU4F3 Is a Common Cause for Autosomal Dominant Nonsyndromic Hearing Loss in Chinese Hans. Neural plasticity 2017 1 2016 9890827. He Longxia, Pang Xiuhong, Chen Penghui, Wu Hao, Yang T |
A Missense Mutation in POU4F3 Causes Midfrequency Hearing Loss in a Chinese ADNSHL Family. BioMed research international 2018 6 2018 5370802. Gao Xue, Xu Jin-Cao, Wang Wei-Qian, Yuan Yong-Yi, Bai Dan, Huang Sha-Sha, Wang Guo-Jian, Su Yu, Li Jia, Kang Dong-Yang, Zhang Mei-Guang, Lin Xi, Dai |
Four Novel Variants in POU4F3 Cause Autosomal Dominant Nonsyndromic Hearing Loss. Neural plasticity 2020 7 2020 6137083. Cui Tian-Yi, Gao Xue, Huang Sha-Sha, Sun Yan-Yan, Zhang Si-Qi, Jiang Xin-Xia, Yang Yan-Zhong, Kang Dong-Yang, Zhu Qing-Wen, Yuan Yong- |
Identification of two novel mutations in POU4F3 gene associated with autosomal dominant hearing loss in Chinese families. Journal of cellular and molecular medicine 2020 (12): 6978-6987. Bai Xiaohui, Zhang Fengguo, Xiao Yun, Jin Yu, Zheng Qingyin, Wang Haibo, Xu L |
[Genetic testing of a Chinese pedigree affected with non-syndromic autosomal dominant deafness 15]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2021 7 38 (7): 639-642. Kang Hongfei, Zhao Kaihui, Kong Xiangdo |
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