Results 141 to 150 of about 1,391 (157)
Some of the next articles are maybe not open access.

High carrier frequency of the 35delG deafness mutation in European populations

European Journal of Human Genetics, 2000
Raquel Rabionet   +2 more
exaly  

Prevalence of c.35delG and p.M34T mutations in the gene in Estonia

International Journal of Pediatric Otorhinolaryngology, 2010
Neeme Tõnisson   +2 more
exaly  

(connexin 26) gene mutations in Moroccan patients with autosomal recessive non-syndromic hearing loss and carrier frequency of the common GJB2–35delG mutation

International Journal of Pediatric Otorhinolaryngology, 2007
Masmoudi Saber   +2 more
exaly  

Prevalence of the 35delG mutation in deaf South Brazilian infants submitted to cochlear implantation

International Journal of Pediatric Otorhinolaryngology, 2012
Liliane Todeschini de Souza   +2 more
exaly  

The analysis of three markers flanking gene suggests a single origin of the most common 35delG mutation in the Moroccan population

Biochemical and Biophysical Research Communications, 2008
Hassan Rouba   +2 more
exaly  

Did the GJB2 35delG mutation originate in Iran?†

American Journal of Medical Genetics, Part A, 2011
Fatemehsadat Esteghamat   +2 more
exaly  

Prevalence of 35delG and Met34Thr variants in Portuguese samples

International Journal of Pediatric Otorhinolaryngology, 2015
Henrique Barros   +2 more
exaly  

Determination of the carrier frequency of the common GJB2 (connexin-26) 35delG mutation in the Greek Cypriot population

International Journal of Pediatric Otorhinolaryngology, 2006
Vassos Neocleous
exaly  

Common mutation analysis of and genes in affected families with autosomal recessive non-syndromic hearing loss from Iran: Simultaneous detection of two common mutations (35delG/del(-D13S1830)) in the DFNB1-related deafness

International Journal of Pediatric Otorhinolaryngology, 2007
Mortaza Bonyadi
exaly  

Connexin 26 mutation 35delG: Prevalence of carriers in various regions in France

International Journal of Pediatric Otorhinolaryngology, 2005
Geraldine Mercier, Gérard Lucotte
exaly  
gjb2
deafness
gjb2 gene
connexin 26
hearing loss
public aspects of medicine
mutation
autosomal recessive non-syndromic hearing loss
genetics
previous   13  14  15  16  

Home - About - Disclaimer - Privacy