Large scale newborn deafness genetic screening of 142,417 neonates in Wuhan, China
Author:
Publisher
Public Library of Science (PLoS)
Subject
Multidisciplinary
Reference74 articles.
1. Hereditary deafness and phenotyping in humans;M Bitnerglindzicz;British Medical Bulletin,2002
2. Genetics of hearing and deafness;S Angeli;Anatomical record,2012
3. An Clinical Research on Newborn Hearing Concurrent Genetic Screening in 106,513 Neonates;B Han;Chinese Journal of Otology,2013
4. Newborn hearing screening—a silent revolution;CC Morton;New England Journal of Medicine,2006
5. Prevalence of permanent childhood hearing impairment in the United Kingdom and implications for universal neonatal hearing screening: questionnaire based ascertainment study;HM Fortnum;Bmj,2001
Cited by 27 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. Economic evaluation of newborn deafness gene screening as a public health intervention in China: a modelling study;BMJ Public Health;2024-04
2. Multicolor melting curve analysis discloses high carrier frequency of hearing loss‐associated variants among neonates in Jiangsu province;Molecular Genetics & Genomic Medicine;2024-02
3. Analysis of deafness susceptibility gene of neonates in northern Guangdong, China;Scientific Reports;2024-01-03
4. Comparative analysis of allele frequencies of 15 deafness gene variants between hearing-loss and normal populations in Henan, China;Heliyon;2023-11
5. Characteristics of hearing loss-associated gene mutations: A multi-center study of 119,606 neonates in Gannan;International Journal of Pediatric Otorhinolaryngology;2023-11
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