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浏览/检索结果: 共5条，第1-5条 帮助 限定条件 学科主题：otorhinolaryngology     已选(0)清除 条数/页：5101520253035404550556065707580859095100   排序方式：请选择发表日期升序发表日期降序提交时间升序提交时间降序题名升序题名降序作者升序作者降序 Common molecular etiology of nonsyndromic hearing loss in 484 patients of 3 ethnicities in northwest China 期刊论文 ACTA OTO-LARYNGOLOGICA, 2015, 卷号: 135, 期号: 6, 页码: 586-591 作者:  Duan, SH;  Zhu, YM;  Wang, YL;  Guo, YF;  Guo, YF (reprint author), Lanzhou Univ, Hosp 2, Dept Otolaryngol Head & Neck Surg, 82 Cuiyingmen St, Lanzhou 730030, Gansu, Peoples R China. 收藏  |  浏览/下载：3/0  |  提交时间：2017/01/10 Deafness-related genes  GJB2  SLC26A4  mtDNA1555A > G  Han Chinese  Hui people  Tibetan   The deafness-causing mutation c.508_511dup in the GJB2 gene and a literature review 期刊论文 ACTA OTO-LARYNGOLOGICA, 2015, 卷号: 135, 期号: 9, 页码: 914-918 作者:  Zhu, YM;  Li, Y;  Wang, YL;  Bian, PP;  Xu, BC 收藏  |  浏览/下载：3/0  |  提交时间：2017/01/10 Frame-shift mutation  GJB2  hearing loss  nomenclature   Prevalence of GJB2 mutations in the Silk Road region of China and a report of three novel variants 期刊论文 ACTA OTO-LARYNGOLOGICA, 2014, 卷号: 134, 期号: 4, 页码: 373-381 作者:  Du, W;  Zhu, YM;  Guo, YF;  Wang, QJ;  Liu, XW 收藏  |  浏览/下载：4/0  |  提交时间：2016/03/29 Hearing loss  genetics  hotspot mutation   Common molecular etiology of patients with nonsyndromic hearing loss in Tibetan, Tu nationality, and Mongolian patients in the northwest of China 期刊论文 ACTA OTO-LARYNGOLOGICA, 2013, 卷号: 133, 期号: 9, 页码: 930-934 作者:  Yang, XL;  Xu, BC;  Chen, XJ;  Bian, PP;  Ma, JL 收藏  |  浏览/下载：4/0  |  提交时间：2016/03/29 Genetic screening  deafness-related genes  genetic counseling   GJB2, SLC26A4 and mitochondrial DNA A1555G mutations in prelingual deafness in Northern Chinese subjects 期刊论文 ACTA OTO-LARYNGOLOGICA, 2008, 卷号: 128, 期号: 3, 页码: 297-303 作者:  Guo, YF;  Liu, XW;  Guan, J;  Han, MK;  Wang, DY 收藏  |  浏览/下载：4/0  |  提交时间：2016/03/29 prelingual deafness  non-syndromic hearing loss  genetic testing  Chinese