Panel-based NGS reveals disease-causing mutations in hearing loss patients using BGISEQ-500 platform-Reference-Cited by-同舟云学术

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Panel-based NGS reveals disease-causing mutations in hearing loss patients using BGISEQ-500 platform

Published:2019-03 Issue:12 Volume:98 Page:e14860
ISSN:0025-7974
Container-title:Medicine
language:en
Short-container-title:

Author:

Sun Yan,Yuan Jing,Wu Limin,Li Min,Cui Xiaoli,Yan Chengbin,Du Lique,Mao Liangwei,Man Jianfen,Li Wei,Kristiansen Karsten,Wu Xuan,Pan Weijun,Yang Yun

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

General Medicine

Reference27 articles.

1. Genetic counseling for patients with nonsyndromic hearing impairment directed by gene analysis;Ma;Mol Med Rep,2016

2. Universal newborn hearing screenings: a three-year experience;Barsky-Firkser;Pediatrics,1997

3. Language ability after early detection of permanent childhood hearing impairment;Kennedy;New Engl J Med,2006

4. Language of early- and later-identified children with hearing loss;Yoshinaga-Itano;Pediatrics,1998

5. Human nonsyndromic sensorineural deafness;Friedman;Annu Rev Genomics Hum Genet,2003

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