Comprehensive genetic testing in the clinical evaluation of 1119 patients with hearing loss-Reference-Cited by-同舟云学术

Comprehensive genetic testing in the clinical evaluation of 1119 patients with hearing loss

Published:2016-03-11 Issue:4 Volume:135 Page:441-450
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Sloan-Heggen Christina M.,Bierer Amanda O.,Shearer A. Eliot,Kolbe Diana L.,Nishimura Carla J.,Frees Kathy L.,Ephraim Sean S.,Shibata Seiji B.,Booth Kevin T.,Campbell Colleen A.,Ranum Paul T.,Weaver Amy E.,Black-Ziegelbein E. Ann,Wang Donghong,Azaiez Hela,Smith Richard J. H.

Funder

National Institute on Deafness and Other Communication Disorders

National Institute of General Medical Sciences

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/s00439-016-1648-8.pdf

Reference34 articles.

1. Bazazzadegan N et al (2012) The spectrum of GJB2 mutations in the Iranian population with non-syndromic hearing loss–a twelve year study. Int J Pediatr Otorhinolaryngol 76:1164–1174. doi: 10.1016/j.ijporl.2012.04.026

2. Blankenberg D et al. (2010) Galaxy: a web-based genome analysis tool for experimentalists. Curr Protoc Mol Biol 10:11–21. doi: 10.1002/0471142727.mb1910s89 (Chapter 19:Unit 19)