CORC

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G59S mutation in the GJB2 gene in a Chinese family with classic Vohwinkel syndrome 期刊论文
JOURNAL OF DERMATOLOGY, 2019, 卷号: Vol.46 No.2, 页码: 154-157
作者:  Xie, Ming-xing;  Yang, Wei-ping;  Luo, Hao-jie;  Ismail, Ferina;  Hao, Yang-yang
收藏  |  浏览/下载:7/0  |  提交时间:2019/12/17
Correlation analysis on clinical effects of acupuncture for elderly patients with sensorineural deafness and ear distending sensation 期刊论文
JOURNAL OF ACUPUNCTURE AND TUINA SCIENCE, 2018, 卷号: 16, 期号: 4
作者:  Mo Wen-quan;  Chu Wen-hao;  Yang Hui;  Wang Jie;  Pei Jian
收藏  |  浏览/下载:13/0  |  提交时间:2019/12/05
Correlation analysis on clinical effects of acupuncture for elderly patients with sensorineural deafness and ear distending sensation 期刊论文
JOURNAL OF ACUPUNCTURE AND TUINA SCIENCE, 2018, 卷号: 16, 期号: 4
作者:  Mo Wen-quan;  Chu Wen-hao;  Yang Hui;  Wang Jie;  Pei Jian
收藏  |  浏览/下载:2/0  |  提交时间:2019/12/05
A homozygous missense variant in HSD17B4 identified in a consanguineous Chinese Han family with type II Perrault syndrome 期刊论文
BMC MEDICAL GENETICS, 2017, 卷号: 18
作者:  Chen, Kui;  Yang, Ke;  Luo, Su-Shan;  Chen, Chen;  Wang, Ying
收藏  |  浏览/下载:4/0  |  提交时间:2019/12/05
Prevalence of Mutations in Deafness-Causing Genes in Cochlear Implanted Patients with Profound Nonsyndromic Sensorineural Hearing Loss in Shandong Province, China 期刊论文
ANNALS OF HUMAN GENETICS, 2017, 卷号: 81, 期号: 6, 页码: 258-266
作者:  Luo, Jianfen;  Bai, Xiaohui;  Zhang, Fengguo;  Xiao, Yun;  Gu, Lintao
收藏  |  浏览/下载:7/0  |  提交时间:2019/12/12
A Novel De novo GATA-binding Protein 3 Mutation in a Patient with Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia Syndrome 期刊论文
2017, 卷号: 130, 期号: 11, 页码: 1378-1380
作者:  Chu Xue-Ying;  Li Yue-Peng;  Nie Min;  Wang Ou;  Jiang Yan
收藏  |  浏览/下载:8/0  |  提交时间:2020/01/04
The relationship between hearing loss and vestibular dysfunction in patients with sudden sensorineural hearing loss 期刊论文
ACTA OTO-LARYNGOLOGICA, 2016, 卷号: 136, 期号: [db:dc_citation_issue], 页码: 225-231
作者:  Niu, Xiaorong;  Zhang, Yan;  Zhang, Qing;  Xu, Xinda;  Han, Peng
收藏  |  浏览/下载:3/0  |  提交时间:2019/12/02
Novel compound heterozygous mutations in MYO7A gene associated with autosomal recessive sensorineural hearing loss in a Chinese family 期刊论文
INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY, 2016, 卷号: 83, 期号: 4, 页码: 179-185
作者:  Ma, Yalin;  Xiao, Yun;  Zhang, Fengguo;  Han, Yuechen;  Li, Jianfeng
收藏  |  浏览/下载:2/0  |  提交时间:2019/12/16
The relationship between hearing loss and vestibular dysfunction in patients with sudden sensorineural hearing loss 期刊论文
ACTA OTO-LARYNGOLOGICA, 2016, 卷号: 136, 期号: 3
作者:  Niu, Xiaorong;  Zhang, Yan;  Zhang, Qing;  Xu, Xinda;  Han, Peng
收藏  |  浏览/下载:8/0  |  提交时间:2019/12/13
A clinical study of sudden deafness 期刊论文
ACTA OTO-LARYNGOLOGICA, 2015, 卷号: 135, 期号: 10
作者:  Zhang, Xiaotong;  Xu, Xinda;  Ma, Weijun;  Zhang, Qing;  Tong, Busheng
收藏  |  浏览/下载:9/0  |  提交时间:2019/12/05


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