CORC

在结果中检索

CORC

浏览/检索结果: 共19条，第1-10条 帮助

限定条件    
已选(0)清除 条数/页：   排序方式：
The mechanoelectrical transducer channel is not required for regulation of cochlear blood flow during loud sound exposure in mice 期刊论文
SCIENTIFIC REPORTS, 2020, 卷号: 10, 期号: 1
作者:  Burwood, George W. S.;  Dziennis, Suzan;  Wilson, Teresa;  Foster, Sarah;  Zhang, Yuan
收藏  |  浏览/下载：29/0  |  提交时间：2020/12/16
Diagnosis, Intervention, and Prevention of Genetic Hearing Loss 期刊论文
HEARING LOSS: MECHANISMS, PREVENTION AND CURE, 2019, 卷号: 1130
作者:  Yang, Tao;  Guo, Luo;  Wang, Longhao;  Yu, Xiaoyu
收藏  |  浏览/下载：12/0  |  提交时间：2019/12/05
Concurrent Hearing and Genetic Screening of 180,469 Neonates with Follow-up in Beijing, China 期刊论文
2019, 卷号: 105, 期号: 4, 页码: 803-812
作者:  Dai Pu;  Huang Li-Hui;  Wang Guo-Jian;  Gao Xue;  Qu Chun-Yan
收藏  |  浏览/下载：37/0  |  提交时间：2020/01/03
Spectrum of DNA variants for non-syndromic deafness in a large cohort from multiple continents 期刊论文
Human Genetics, 2016, 卷号: 135, 期号: 8, 页码: 953-961
作者:  Yan, Denise;  Tekin, Demet;  Bademci, Guney;  Foster, Joseph, II;  Cengiz, F. Basak
收藏  |  浏览/下载：3/0  |  提交时间：2019/12/03
A study of deafness-related genetic mutations as a basis for strategies to prevent hereditary hearing loss in Hebei, China 期刊论文
Intractable & Rare Diseases Research, 2015, 卷号: Vol.4 No.3, 页码: 131–138
作者:  Junzhen Zhu;  Qinying Cao;  Ning Zhang;  Jun Ge;  Donglan Sun
收藏  |  浏览/下载：2/0  |  提交时间：2019/03/26
A genome-wide search for quantitative trait loci affecting the cortical surface area and thickness of Heschl's gyrus 期刊论文
GENES BRAIN AND BEHAVIOR, 2014, 卷号: 13, 期号: 7, 页码: 675-685
作者:  Cai, D. -C.;  Fonteijn, H.;  Guadalupe, T.;  Zwiers, M.;  Wittfeld, K.
收藏  |  浏览/下载：20/0  |  提交时间：2015/09/09
Whole-Exome Sequencing to Decipher the Genetic Heterogeneity of Hearing Loss in a Chinese Family with Deaf by Deaf Mating 期刊论文
PLOS ONE, 2014, 卷号: 9, 期号: 10, 页码: e109178
作者:  Qing, Jie;  Yan, Denise;  Zhou, Yuan;  Liu, Qiong;  Wu, Weijing
收藏  |  浏览/下载：10/0  |  提交时间：2019/12/03
Combined examination of sequence and copy number variations in human deafness genes improves diagnosis for cases of genetic deafness. 期刊论文
BMC ear, nose, and throat disorders, 2014, 卷号: 14
作者:  Ji Haiting;  Lu Jingqiao;  Wang Jianjun;  Li Huawei;  Lin Xi
收藏  |  浏览/下载：7/0  |  提交时间：2019/12/19
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
Hearing loss and PRPS1 mutations: Wide spectrum of phenotypes and potential therapy 期刊论文
INTERNATIONAL JOURNAL OF AUDIOLOGY, 2013, 卷号: 52, 期号: 1, 页码: 23-28
作者:  Liu, Xue Zhong*;  Xie, Dinghua;  Yuan, Hui Jun;  de Brouwer, Arjan P. M.;  Christodoulou, John
收藏  |  浏览/下载：1/0  |  提交时间：2019/12/03

©版权所有 ©2017 CSpace - Powered by CSpace