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Research article

First published 2022

Analysis of GJB2 Gene Mutations in 1330 Deafness Cases of Major Ethnic Groups in Northwest China

Panpan Bian, Baicheng Xu, Xiaoyun Zhao [...]

INQUIRY: The Journal of Health Care Organization,Provision,and Financing

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Brief report

First published 2001-06

High Frequency of GJB2 Gene Mutations in Polish Patients with Prelingual Nonsyndromic Deafness

Wojciech Wiszniewski, Lucja Sobieszczanska-Radoszewska, Ewa Nowakowska-Szyrwinska [...]

Genetic Testing and Molecular Biomarkers

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Research article

First published 2008-12

Carrier Frequencies of Mutations/Polymorphisms in the Connexin 26 Gene ( GJB2 ) in the Moroccan Population

Omar Abidi, Redouane Boulouiz, Halima Nahili [...]

Genetic Testing and Molecular Biomarkers

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Research article

First published 2011-09

Phenotype-Genotype Correlation in 295 Chinese Deaf Subjects with Biallelic Causative Mutations in the GJB2 Gene

Fei-Fan Zhao, Yu-Bin Ji, Da-Yong Wang [...]

Genetic Testing and Molecular Biomarkers

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Research article

First published 2009-04

Analysis of the GJB2 and GJB6 Genes in Italian Patients with Nonsyndromic Hearing Loss: Frequencies,Novel Mutations,Genotypes,and Degree of Hearing Loss

Paola Primignani, Luca Trotta, Pierangela Castorina [...]

Genetic Testing and Molecular Biomarkers

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Research article

First published 2014-11

Sequencing of GJB2 in Cameroonians and Black South Africans and comparison to 1000 Genomes Project Data Support Need to Revise Strategy for Discovery of Nonsyndromic Deafness Genes in Africans

Jason Bosch, Jean Jacques N. Noubiap, Collet Dandara [...]

OMICS: A Journal of Integrative Biology

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Research article

First published 2007-03

Allelic Frequencies of The 35delG Mutation of The GJB2 Gene in Different Brazilian Regions

C.A. Oliveira, C.J. Pimpinati, F. Alexandrino [...]

Genetic Testing and Molecular Biomarkers

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Research article

First published 2005-03

The 35delG Mutation in the Connexin 26 Gene ( GJB2 ) Associated with Congenital Deafness: European Carrier Frequencies and Evidence for Its Origin in Ancient Greece

Gérard Lucotte, Florent Diéterlen

Genetic Testing and Molecular Biomarkers

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Review article

First published 2001-10

High-Frequency Hearing Loss Correlated With Mutation in the GJB2 Gene

Irwin A. Schafer

Clinical Pediatrics

Free access

Other

First published 2000-09

Rapid detection of the 35delG mutation in the GJB2 gene in childhood deafness

Journal of Medical Screening

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