Genetics of congenital hearing impairment: A clinical approach
Author:
Publisher
Informa UK Limited
Subject
Speech and Hearing,Linguistics and Language,Language and Linguistics
Link
http://www.tandfonline.com/doi/pdf/10.1080/14992020802249259
Reference54 articles.
1. Uniparental disomy of chromosome 13q causing homozygosity for the 35delG mutation in the gene encoding connexin26 (GJB2) results in prelingual hearing impairment in two unrelated Spanish patients
2. Aetiological investigations of hearing loss in childhood: a review
3. Homozygosity for the V37I Connexin 26 mutation in three unrelated children with sensorineural hearing loss
4. Hereditary deafness and phenotyping in humans
5. Language and Speech Perception Outcomes in Hearing-Impaired Children with and without Connexin 26 Mutations
Cited by 19 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. Prevention of Disorders of Hearing Development;Phoniatrics I;2019-12-05
2. Moderate sensorineural hearing loss is typical for DFNB16 caused by various types of mutations affecting the STRC gene;European Archives of Oto-Rhino-Laryngology;2019-09-24
3. Language outcome in children with congenital hearing impairment: The influence of etiology;International Journal of Pediatric Otorhinolaryngology;2019-02
4. Phenotypic Characterization of DFNB16-associated Hearing Loss;Otology & Neurotology;2019-01
5. Two molecular assays for the rapid and inexpensive detection ofGJB2andGJB6mutations;ELECTROPHORESIS;2016-01-15
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