A reverse dot blot assay for the screening of twenty mutations in four genes associated with NSHL in a Chinese population-Reference-Cited by-同舟云学术

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A reverse dot blot assay for the screening of twenty mutations in four genes associated with NSHL in a Chinese population

Published:2017-05-15 Issue:5 Volume:12 Page:e0177196
ISSN:1932-6203
Container-title:PLOS ONE
language:en
Short-container-title:PLoS ONE

Author:

Li Siping,Peng Qi,Liao Shengyun,Li Wenrui,Ma Qiang,Lu Xiaomei^ORCID

Funder

the Dongguan Bureau of Science and Technology for the City Key Program of Science and Technology

the Science and Technology Planning Project of Guangdong Province

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference29 articles.

1. Newborn hearing screening—a silent revolution;CC Morton;New England Journal of Medicine,2006

2. Profound deafness in childhood;A Kral;New England Journal of Medicine,2010

3. Newborn hearing concurrent genetic screening for hearing impairment- a clinical practice in 58,397neonates in Tianjin,china;J Zhang;International Journal of Pediatric Otorhinolaryngology

4. Genes responsible for human hereditary deafness: Symphony of a thousand;C Petit;Nat Genet,1996

5. Genetic causes of hearing loss;PJ Willems;New England Journal of Medicine,2000

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