Results 161 to 170 of about 5,521 (170)

Keratitis-ichthyosis-deafness syndrome in a child with mutations in the GJB2 gene

Chinese Journal of Dermatology, 2021
openaire   +1 more source

Large deletion of theGJB6gene in deaf patients heterozygous for theGJB2gene mutation: Genotypic and phenotypic analysis

2004
Sébastien Schmerber, Christine Petit, Pierre Chauvin   +2 more
exaly  

Novel mutations in the connexin 26 gene (GJB2) responsible for childhood deafness in the Japanese population

American Journal of Medical Genetics Part A, 2000
T Takasaka
exaly  

Changes in the connexin 26 gene (GJB2) in Russian patients with hearing loss: Results of long-term molecular diagnostics of hereditary nonsyndromic hearing loss

Russian Journal of Genetics, 2012
Elena Bliznetz
exaly  

A novel dominant missense mutation - D179N - in the GJB2 gene (Connexin 26) associated with non-syndromic hearing loss

Clinical Genetics, 2003
Domenico Coviello
exaly  

Statistical study of 35delG mutation of GJB2 gene: A meta-analysis of carrier frequency

International Journal of Audiology, 2009
Nejat Mahdieh, Bahareh Rabbani
exaly  

Persistent vertigo secondary to a GJB2 gene alteration

Journal of the Neurological Sciences
openaire   +1 more source

Epidemiology of 35delG mutation in GJB2 gene in a Polish population

Journal of Audiological Medicine, 2001
Mueller-Malesinska, Małgorzata, Nowak, Magdalena, Skarżyński, Henryk, Waligóra, Jarosław, Korniszewski, Lech   +4 more
openaire  

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

Clinical Pediatrics, 2001
openaire   +1 more source

Long-Term Progression of Hearing Loss associated with the mitochondrial gene 3243A>G variant and <i>GJB2</i> gene variant

Audiology Japan
exaly