Nonsyndromic Hearing Loss
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Speech and Hearing,Otorhinolaryngology
Reference125 articles.
1. A human homologue of the Drosophila eyes absent gene underlies branchio-oto-renal (BOR) syndrome and identifies a novel gene family;Abdelhak;Nature Genetics,1997
2. Nonsyndromic recessive deafness DFNB18 and Usher syndrome type IC are allelic mutations of USHIC;Ahmed;Human Genetics,2002
3. The implications of genetic testing for deafness;Arnos;Ear Hearing,2003
4. Mouse models for deafness. Lessons for the human inner ear and hearing loss;Avraham;Ear Hearing,2003
5. The mouse Snell's waltzer deafness gene encodes an unconventional myosin required for structural integrity of inner ear hair cells;Avraham;Nature Genetics,1995
Cited by 48 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. A NOVEL <i>LOXHD1</i> PATHOGENIC VARIANT IN GREECE: CASE STUDY OF A DNFB77 NONSYNDROMIC HEARING IMPAIRMENT;Journal of Hearing Science;2023-12-22
2. Newborn Hearing Screening;Hearing Loss in Congenital, Neonatal and Childhood Infections;2023
3. Genetic linkage analysis of DFNB22 in families with autosomal recessive non-syndromic hearing loss in Khuzestan province;Journal of Shahrekord University of Medical Sciences;2019-10-30
4. Grxcr2 is required for stereocilia morphogenesis in the cochlea;PLOS ONE;2018-08-29
5. The first case of NSHL by direct impression on EYA1 gene and identification of one novel mutation in MYO7A in the Iranian families;IRAN J BASIC MED SCI;2018
1.学者识别学者识别
2.学术分析学术分析
3.人才评估人才评估
"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370
www.globalauthorid.com
TOP
Copyright © 2019-2024 北京同舟云网络信息技术有限公司 京公网安备11010802033243号 京ICP备18003416号-3