Genotyping for Cx26 and Cx30 Mutations in Cases with Congenital Hearing Loss
Author:
Affiliation:
1. Department of Medical Biology, Medical Faculty, Afyonkarahisar Kocatepe University, Afyonkarahisar, Turkey.
2. Department of Otolaryngology, Medical Faculty, Afyonkarahisar Kocatepe University, Afyonkarahisar, Turkey.
Publisher
Mary Ann Liebert Inc
Subject
Genetics(clinical)
Link
http://www.liebertpub.com/doi/pdf/10.1089/gte.2007.0106
Reference18 articles.
1. GJB2 gene mutations causing familial hereditary deafness in Turkey
2. Clinical Studies of Families With Hearing Loss Attributable to Mutations in the Connexin 26 Gene (GJB2/DFNB1)
3. Etiology of deafness in Afyon school for the deaf in Turkey
4. Connexin 26 and Connexin 30 Mutations in Children with Nonsyndromic Hearing Loss
Cited by 10 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. Role of GJB2 and GJB6 in Iranian Nonsyndromic Hearing Impairment: From Molecular Analysis to Literature Reviews;Fetal and Pediatric Pathology;2019-06-19
2. Bilateral congenital deafness: What investigations should be performed?;Swiss Medical Weekly;2017-03-03
3. GJB2 and GJB6 genes mutations in children with non-syndromic hearing loss;Revista Romana de Medicina de Laborator;2017-02-18
4. Detection of 35delG, 167delT mutations in the connexin 26 gene among Egyptian patients with nonsyndromic sensorineural hearing loss;The Egyptian Journal of Otolaryngology;2015-01
5. Prenatal Screening for the35delG GJB2, Del (GJB6-D13S1830), and Del (GJB6-D13S1854) Mutations in the Romanian Population;Genetic Testing and Molecular Biomarkers;2011-11
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