Results 121 to 130 of about 675 (134)

GJB2 mutations in Iranian Azeri population with autosomal recessive nonsyndromic hearing loss (ARNSHL): First report of c.238 C>A mutation in Iran

Journal of Clinical Laboratory Analysis, 2021
Bahareh Rahimi, Behzad Davarnia, Haleh Mokabber   +2 more
exaly  

Prevalence of IVS1+1G>A mutation among Iranian Azeri Turkish patients with autosomal recessive non-syndromic hearing loss (ARNSHL)

International Journal of Pediatric Otorhinolaryngology, 2011
Mortaza Bonyadi, Níkou Fotouhi
exaly  

Mutation Screening of Exons 7 and 13 of the TMC1 Gene in Autosomal Recessive Non-syndromic Hearing Loss (ARNSHL) in Iran

Iranian Red Crescent Medical Journal, 2016
Morteza Hashemzadeh-Chaleshtori, Payam Ghasemi-Dehkordi, Ahmad Rashki   +2 more
exaly  

The Prevalence of Connexin 26 Mutations in the Swedish Population

Audiological Medicine, 2005
Christina Hederstierna, Ulrika von Döbeln, Claes Möller   +2 more
exaly  

Did the GJB2 35delG mutation originate in Iran?

American Journal of Medical Genetics, Part A, 2011
Fatemehsadat Esteghamat, Niloofar Bazazzadegan, Hossein Najmabadi   +2 more
exaly  

Screening of OTOF mutations in Iran: A novel mutation and review

International Journal of Pediatric Otorhinolaryngology, 2012
Mohammad Taghi Akbari, Mustafa Tekin, Nejat Mahdieh   +2 more
exaly  

Whole-Exome Sequencing Identifies a Variant inTMEM132ECausing Autosomal-Recessive Nonsyndromic Hearing Loss DFNB99

Human Mutation, 2015
Changshun Shao
exaly  

Common mutation analysis of GJB2 and GJB6 genes in affected families with autosomal recessive non-syndromic hearing loss from Iran: Simultaneous detection of two common mutations (35delG/del(GJB6-D13S1830)) in the DFNB1-related deafness

International Journal of Pediatric Otorhinolaryngology, 2007
Mortaza Bonyadi
exaly  

A novel pathogenic variant in the MARVELD2 gene causes autosomal recessive non-syndromic hearing loss in an Iranian family

Genomics, 2019
Morteza Hashemzadeh-Chaleshtori, Javad Mohammadi-Asl, Mohammad Amin Tabatabaiefar   +2 more
exaly  

miRNA mutations are not a common cause of deafness

American Journal of Medical Genetics, Part A, 2010
Hossein Najmabadi, Richard Smith, Michael Hildebrand   +2 more
exaly