Human Genome Epidemiology Literature Finder
Records 1 - 6 (of 6 Records) |
Query Trace: Attention and GJB2[original query] |
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GJB2 mutations and additional disabilities in a pediatric cochlear implant population. International journal of pediatric otorhinolaryngology 2006 Mar 70 (3): 493-500. Wiley S, Choo D, Meinzen-Derr J, Hilbert L, Greinwald |
[Prevalence of common genetic mutations and clinical characteristics analysis in patients at different ages with nonsyndromic hearing impairment]. Yi chuan = Hereditas / Zhongguo yi chuan xue hui bian ji 2013 Mar 35 (3): 352-8. Zhang Chu-Qin, Chen Bo-Bei, Chen Ying-Ying, Liu Xue-Jun, Zheng Jing, Gao Jin-Jian, Huang Sai-Yu, Nan Ben-Yu, Zhang Yu-Yao, Yu Xiao, Guan Min-X |
DFNB16 is a frequent cause of congenital hearing impairment: implementation of STRC mutation analysis in routine diagnostics. Clinical genetics 2015 87 (1): 49-55. Vona B, Hofrichter M A H, Neuner C, Schröder J, Gehrig A, Hennermann J B, Kraus F, Shehata-Dieler W, Klopocki E, Nanda I, Haaf |
The Analysis of A Frequent TMPRSS3 Allele Containing P.V116M and P.V291L in A Cis Configuration among Deaf Koreans. International journal of molecular sciences 2017 Oct 18 (11): . Kim Ah Reum, Chung Juyong, Kim Nayoung K D, Lee Chung, Park Woong-Yang, Oh Doo-Yi, Choi Byung Yo |
Analysis between phenotypes and genotypes of inner ear malformation. Acta oto-laryngologica 2019 2 139 (3): 223-232. Wang Suyang, Ding Wenjuan, Chen Chi, Xu Baicheng, Liu Xiaowen, Bian Panpan, Guo Yuf |
Hearing Phenotypes of Patients with Hearing Loss Homozygous for the GJB2 c.235delc Mutation. Neural plasticity 2020 8 2020 8841522. Guo Chang, Huang Sha-Sha, Yuan Yong-Yi, Zhou Ying, Wang Ning, Kang Dong-Yang, Yang Su-Yan, Zhang Xin, Gao Xue, Dai |
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