Genetic etiology study of the non-syndromic deafness in Chinese Hans by targeted next-generation sequencing

Targeted massive parallel sequencing: the effective detection of novel causative mutations associated with hearing loss in small families

(2012) Jeong-In Baek et al.   Orphanet Journal of Rare Diseases

Molecular Epidemiology and Functional Assessment of Novel Allelic Variants of SLC26A4 in Non-Syndromic Hearing Loss Patients with Enlarged Vestibular Aqueduct in China

(2012) Yongyi Yuan et al.   PLoS One

Targeted genomic capture and massively parallel sequencing to identify genes for hereditary hearing loss in middle eastern families

(2011) Zippora Brownstein et al.   GENOME BIOLOGY

Molecular epidemiological analysis of mitochondrial DNA12SrRNA A1555G,GJB2,andSLC26A4mutations in sporadic outpatients with nonsyndromic sensorineural hearing loss in China

(2010) Yu-bin Ji et al.   ACTA OTO-LARYNGOLOGICA

A novel mutation adjacent to theBthmouse mutation in theTMC1gene makes this mouse an excellent model of human deafness at the DFNA36 locus

(2010) T Yang et al.   CLINICAL GENETICS

Comprehensive genetic testing for hereditary hearing loss using massively parallel sequencing

(2010) A. E. Shearer et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

GJB2 mutation spectrum in 2063 Chinese patients with nonsyndromic hearing impairment

(2009) Pu Dai et al.   Journal of Translational Medicine