Pregestational screening of hereditary deafness genes carriers in 10,684 normal pregnant women in Zhuzhou , China

Mutation analysis of common deafness genes among 1,201 patients with non‐syndromic hearing loss in Shanxi Province

(2019) Yongan Zhou et al.   Molecular Genetics & Genomic Medicine

Mutation spectrum and hotspots of the common deafness genes in 314 patients with nonsyndromic hearing loss in Heze area, China

(2019) Meng Zhang et al.   ACTA OTO-LARYNGOLOGICA

SLC26A4-linked CEVA haplotype correlates with phenotype in patients with enlargement of the vestibular aqueduct

(2019) Janet R. Chao et al.   BMC Medical Genetics

Mutation analysis of common deafness-causing genes among 506 patients with nonsyndromic hearing loss from Wenzhou city, China

(2019) Yan-bao Xiang et al.   INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY

Variations in the Mutational Spectrum in Nonsyndromic Hearing Impairment: A study of the Special Schools for the Deaf in Southern China

(2019) Ying Lin et al.   Journal of International Advanced Otology

World Health Organization and Its Initiative for Ear and Hearing Care

(2018) Shelly Chadha et al.   OTOLARYNGOLOGIC CLINICS OF NORTH AMERICA

Common and Founder Mutations for Monogenic Traits in Sub-Saharan African Populations

(2018) Amanda Krause et al.   Annual Review of Genomics and Human Genetics

The relationship between the GJB3 c.538C>T variant and hearing phenotype in the Chinese population

(2017) Shasha Huang et al.   INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY

GJB2 as Well as SLC26A4 Gene Mutations are Prominent Causes for Congenital Deafness

(2015) Yuan Fang et al.   CELL BIOCHEMISTRY AND BIOPHYSICS

The Genetic Basis of Nonsyndromic Hearing Loss in Indian and Pakistani Populations

(2015) Denise Yan et al.   Genetic Testing and Molecular Biomarkers

Screening and analysis of mutation hot-spots in deafness-associated genes among adolescents with hearing loss

(2015) HONG JIANG et al.   Molecular Medicine Reports

Analysis of common deafness gene mutations in deaf people from unique ethnic groups in Gansu Province, China

(2014) Bai-Cheng Xu et al.   ACTA OTO-LARYNGOLOGICA

Global and regional hearing impairment prevalence: an analysis of 42 studies in 29 countries

(2011) Gretchen Stevens et al.   EUROPEAN JOURNAL OF PUBLIC HEALTH

GJB2 mutation spectrum in 2063 Chinese patients with nonsyndromic hearing impairment

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