Common Molecular Etiologies Are Rare in Nonsyndromic Tibetan Chinese Patients with Hearing Impairment

Cochlear Implantation in Children with Congenital X-Linked Deafness Due to Novel Mutations in POU3F4 Gene

(2014) Konstantina M. Stankovic et al.   ANNALS OF OTOLOGY RHINOLOGY AND LARYNGOLOGY

Impact of Consanguineous Marriages in GJB2-Related Hearing Loss in the Iranian Population: A Report of a Novel Variant

(2011) Nejat Mahdieh et al.   Genetic Testing and Molecular Biomarkers

A large cohort study ofGJB2mutations in Japanese hearing loss patients

(2010) K Tsukada et al.   CLINICAL GENETICS

Identification of a novel mutation in POU3F4 for prenatal diagnosis in a Chinese family with X-linked nonsyndromic hearing loss

(2010) Jianzhong Li et al.   Journal of Genetics and Genomics

Genetic Evidence for High-Altitude Adaptation in Tibet

(2010) T. S. Simonson et al.   SCIENCE

NovelPOU3F4mutations and clinical features of DFN3 patients with cochlear implants

(2009)   CLINICAL GENETICS

Mutation Analysis of Familial GJB2-Related Deafness in Iranian Azeri Turkish Patients

(2009) Mortaza Bonyadi et al.   Genetic Testing and Molecular Biomarkers

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

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

Carrier frequency of GJB2 (connexin-26) mutations causing inherited deafness in the Korean population

(2008) Sung-Hee Han et al.   JOURNAL OF HUMAN GENETICS