Deafness gene mutations in newborns in Beijing-Reference-Cited by-同舟云学术

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Deafness gene mutations in newborns in Beijing

Published:2016-01-14 Issue:5 Volume:136 Page:475-479
ISSN:0001-6489
Container-title:Acta Oto-Laryngologica
language:en
Short-container-title:Acta Oto-Laryngologica

Author:

Han Shujing,Yang Xiaojian,Zhou Yi,Hao Jinsheng,Shen Adong,Xu Fang,Chu Ping,Jin Yaqiong,Lu Jie,Guo Yongli,Shi Jin,Liu Haihong,Ni Xin

Publisher

Informa UK Limited

Subject

Otorhinolaryngology,General Medicine

Link

http://www.tandfonline.com/doi/pdf/10.3109/00016489.2015.1128121

Reference20 articles.

1. Newborn Hearing Screening — A Silent Revolution

2. Genetic epidemiological studies of early-onset deafness in the U.S. school-age population

3. Deafness Genes and Their Diagnostic Applications

4. Forty-six genes causing nonsyndromic hearing impairment: Which ones should be analyzed in DNA diagnostics?

5. Comprehensive molecular etiology analysis of nonsyndromic hearing impairment from typical areas in China

Cited by 9 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. Characteristics of hearing loss-associated gene mutations: A multi-center study of 119,606 neonates in Gannan;International Journal of Pediatric Otorhinolaryngology;2023-11

2. Incidence and trend of preterm birth in China, 1990–2016: a systematic review and meta-analysis;BMJ Open;2020-12

3. Combined hearing screening and genetic screening of deafness among Hakka newborns in China;International Journal of Pediatric Otorhinolaryngology;2020-09

4. The prevalence of deafness-associated mutations in neonates: A meta-analysis of clinical trials;International Journal of Pediatric Otorhinolaryngology;2019-06

5. Two Compound Heterozygous Were Identified in SLC26A4 Gene in Two Chinese Families With Enlarged Vestibular Aqueduct;Clinical and Experimental Otorhinolaryngology;2019-02-01

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