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

GJB2, SLC26A4, and mitochondrialDNA12S rRNAhot-spots in 156 subjects with non-syndromic hearing loss in Tengzhou, China

(2016) Yalin Ma et al.   ACTA OTO-LARYNGOLOGICA

Analysis of mitochondrial alterations in Brazilian patients with sensorineural hearing loss using MALDI-TOF mass spectrometry

(2016) Rogério Marins Alves et al.   BMC Medical Genetics

Molecular newborn screening of four genetic diseases in Guizhou Province of South China

(2016) Shengwen Huang et al.   GENE

Concurrent Genetic and Standard Screening for Hearing Impairment in 9317 Southern Chinese Newborns

(2016) Qi Peng et al.   Genetic Testing and Molecular Biomarkers

Application of a New Genetic Deafness Microarray for Detecting Mutations in the Deaf in China

(2016) Hong Wu et al.   PLoS One

A rapid method for simultaneous multi-gene mutation screening in children with nonsyndromic hearing loss

(2014) Wan Du et al.   GENOMICS

Novel mutations ofSLC26A4in Chinese patients with nonsyndromic hearing loss

(2013) Gendong Yao et al.   ACTA OTO-LARYNGOLOGICA

Newborn hearing concurrent genetic screening for hearing impairment—A clinical practice in 58,397 neonates in Tianjin, China

(2013) Junqing Zhang et al.   INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY

Genetic mutations in nonsyndromic deafness patients of Chinese minority and han ethnicities in Yunnan, China

(2013) Feng Xin et al.   Journal of Translational Medicine

Profound Deafness in Childhood

(2010) Andrej Kral et al.   NEW ENGLAND JOURNAL OF MEDICINE

Molecular Etiology of Hearing Impairment in Inner Mongolia: mutations in SLC26A4 gene and relevant phenotype analysis

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

Comprehensive molecular etiology analysis of nonsyndromic hearing impairment from typical areas in China

(2009) Yongyi Yuan et al.   Journal of Translational Medicine

GJB2 mutation spectrum in 2063 Chinese patients with nonsyndromic hearing impairment

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