Results 191 to 200 of about 8,250 (205)

Progressive hearing loss, and recurrent sudden sensorineural hearing loss associated with GJB2 mutations – phenotypic spectrum and frequencies of GJB2 mutations in Austria

Human Genetics, 2002
Gerd Utermann, Barbara Utermann, Judith Löffler   +2 more
exaly  

GJB2 (connexin 26) variants and nonsyndromic sensorineural hearing loss: A HuGE review

Genetics in Medicine, 2002
Kim Van Naarden Braun, Aileen Kenneson, Coleen Boyle   +2 more
exaly  

Ethnic-Specific Spectrum of GJB2 and SLC26A4 Mutations: Their Origin and a Literature Review

Annals of Otology, Rhinology and Laryngology, 2015
Shin-Ya Nishio, Shin-Ichi Usami, Keita Tsukada   +2 more
exaly  

The prevalence of connexin 26 (GJB2) mutations in the Chinese population

Human Genetics, 2002
Xue Zhong Liu, Xuezhong Liu, Xiao Mei Ouyang   +2 more
exaly  

GJB2-related hearing loss in central Iran: Review of the spectrum and frequency of gene mutations

Annals of Human Genetics, 2020
Fatemeh Azadegan-Dehkordi, Mahboobeh Koohiyan, Mahbobeh Koohiyan   +2 more
exaly  

Connexin 26 (GJB2) Mutations Associated with Non-Syndromic Hearing Loss (NSHL)

Indian Journal of Pediatrics, 2018
Shubha R Phadke, Priyanka Srivastava, Kausik Mandal   +2 more
exaly  

GJB2 deafness gene shows a specific spectrum of mutations in Japan, including a frequent founder mutation

Human Genetics, 2003
Guy Van Camp, Shin-Ichi Usami, Lut Van Laer   +2 more
exaly  

Low frequency of deafness-associated GJB2 variants in Kenya and Sudan and novel GJB2 variants†‡

Human Mutation, 2004
Nagla Gasmelseed, Rolf D Horstmann
exaly  

Absence of deafness-associated connexin-26 (GJB2) gene mutations in the Omani population † ‡

Human Mutation, 2001
Muralitharan Shanmugakonar, Nadia Mohammed Al-Wardy, M Simsek   +2 more
exaly  

Higher brain functions of GJB2-associated deafness

International Journal of Pediatric Otorhinolaryngology, 2007
openaire   +2 more sources