Mutational analysis of the SLC26A4 gene in Chinese sporadic nonsyndromic hearing-impaired children-Reference-Cited by-同舟云学术

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Mutational analysis of the SLC26A4 gene in Chinese sporadic nonsyndromic hearing-impaired children

Published:2012-10 Issue:10 Volume:76 Page:1474-1480
ISSN:0165-5876
Container-title:International Journal of Pediatric Otorhinolaryngology
language:en
Short-container-title:International Journal of Pediatric Otorhinolaryngology

Author:

Hu Xiangyang,Liang Fenghe,Zhao Min,Gong Angela,Berry Emily R.,Shi Yang,Wang Yanxiao,Chen Yan,Liu Aishu,Qu Chunyan

Publisher

Elsevier BV

Subject

Otorhinolaryngology,General Medicine,Pediatrics, Perinatology and Child Health

Reference46 articles.

1. Hereditary hearing loss;Petit,2001

2. Universal infant hearing screening by automated auditory brainstem response measurement;Mason;Pediatrics,1998

3. The need for universal neonatal hearing screening – some aspects of epidemiology and identification;Parving;Acta Paediatr. Suppl.,1999

4. Newborn hearing concurrent gene screening can improve care for hearing loss: a study on 14,913 Chinese newborns;Wang;Int. J. Pediatr. Otorhinolaryngol.,2011

5. Sensorineural hearing loss in children;Smith;Lancet,2005

Cited by 14 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. Genetics of Inner Ear Malformations: A Review;Audiology Research;2021-10-12

2. Genetic Determinants of Non-Syndromic Enlarged Vestibular Aqueduct: A Review;Audiology Research;2021-08-28

3. A Mutational Analysis of GJB2, SLC26A4, MT-RNA1, and GJB3 in Children with Nonsyndromic Hearing Loss in the Henan Province of China;Genetic Testing and Molecular Biomarkers;2019-01

4. Analysis of mutation spectrum of common deafness-causing genes in Hakka newborns in southern China by semiconductor sequencing;Medicine;2018-09

5. Noninvasive and Accurate Detection of Hereditary Hearing Loss Mutations with Buccal Swab Based on Droplet Digital PCR;Analytical Chemistry;2018-07-10

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