CORC

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CORC

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Two Compound Heterozygous Were Identified in SLC26A4 Gene in Two Chinese Families With Enlarged Vestibular Aqueduct 期刊论文
CLINICAL AND EXPERIMENTAL OTORHINOLARYNGOLOGY, 2019, 卷号: Vol.12 No.1, 页码: 50
作者:  Yu, Yongbo;  Yang, Yang;  Lu, Jie;  Jin, Yaqiong;  Yang, Yeran
收藏  |  浏览/下载：5/0  |  提交时间：2019/12/17
Genotyping and audiological characteristics of infants with a single-allele SLC26A4 mutation. 期刊论文
International journal of pediatric otorhinolaryngology, 2019, 卷号: Vol.116, 页码: 153-158
作者:  Zhao Xuelei;  Huang Lihui;  Wang Xueyao;  Wang Xianlei;  Zhao Liping
收藏  |  浏览/下载：4/0  |  提交时间：2019/12/13
Identification of SLC26A4 mutations p.L582LfsX4, p.I188T and p.E704K in a Chinese family with large vestibular aqueduct syndrome (LVAS) 期刊论文
INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY, 2016, 卷号: 91
作者:  Li, Yunlong;  Zhu, Baosheng;  Su, Jie;  Yin, Yifei;  Yu, Fangqing
收藏  |  浏览/下载：8/0  |  提交时间：2019/12/04
Identification of a novel mutation in SLC26A4 gene in a Chinese family with enlarged vestibular aqueduct syndrome 期刊论文
INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY, 2016, 卷号: 85, 页码: 75-79
作者:  Zhang, Fengguo;  Bai, Xiaohui;  Xiao, Yun;  Zhang, Xue;  Zhang, Guodong
收藏  |  浏览/下载：3/0  |  提交时间：2019/12/16
Novel compound heterozygous mutations in SLC26A4 gene in a Chinese Han family with enlarged vestibular aqueduct 期刊论文
INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY, 2016, 卷号: 90, 页码: 170-174
作者:  Wang, Mingming;  Zhang, Fengguo;  Xu, Lei;  Xiao, Yun;  Li, Jianfeng
收藏  |  浏览/下载：5/0  |  提交时间：2019/12/16
A rapid method for simultaneous multi-gene mutation screening in children with nonsyndromic hearing loss 期刊论文
GENOMICS, 2014, 卷号: 104, 期号: 4, 页码: 264-270
作者:  Du, W;  Cheng, J;  Ding, H;  Jiang, ZW;  Guo, YF
收藏  |  浏览/下载：4/0  |  提交时间：2016/03/29
Analysis of common deafness gene mutations in deaf people from unique ethnic groups in Gansu Province, China 期刊论文
ACTA OTO-LARYNGOLOGICA, 2014, 卷号: 134, 期号: 9, 页码: 924-929
作者:  Xu, BC;  Bian, PP;  Liu, XW;  Zhu, YM;  Yang, XL
收藏  |  浏览/下载：4/0  |  提交时间：2016/03/29
A systematic review and meta-analysis of common mutations of SLC26A4 gene in Asian populations 期刊论文
INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY, 2013, 卷号: 77, 期号: 10, 页码: 1670-1676
作者:  Du, W;  Guo, YF;  Wang, CL;  Wang, YL;  Liu, XW
收藏  |  浏览/下载：4/0  |  提交时间：2016/03/29
Newborn hearing concurrent gene screening can improve care for hearing loss: A study on 14,913 Chinese newborns 期刊论文
INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY, 2011, 卷号: 75, 期号: 4, 页码: 535-542
作者:  Wang, QJ;  Zhao, YL;  Rao, SQ;  Guo, YF;  He, Y
收藏  |  浏览/下载：3/0  |  提交时间：2016/03/29
基因芯片技术在非综合征性耳聋快速基因诊断中的应用研究 期刊论文
2010, 2010
王国建; 戴朴; 韩东一; 李彩霞; 张地; 韩冰; 康东洋; 张昕; WANG Guo-jian; DAI Pu; HAN Dong-yi; LI Cai-xia; ZHANG Di; HAN Bing; KANG Dong-yang; ZHANG Xin
收藏  |  浏览/下载：3/0

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