Results 141 to 150 of about 7,994 (153)

A distinct spectrum of SLC26A4 mutations in patients with enlarged vestibular aqueduct in China

Clinical Genetics, 2007
Y-L Zhao
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  

Functional Testing of SLC26A4 Variants—Clinical and Molecular Analysis of a Cohort with Enlarged Vestibular Aqueduct from Austria

International Journal of Molecular Sciences, 2018
Miklós Tóth, Wolfgang Patsch, Emanuele Bernardinelli   +2 more
exaly  

Audiologic presentation of enlargement of the vestibular aqueduct according to the SLC26A4 genotypes

Laryngoscope, 2015
Byung Yoon Choi, Ja Won Koo, Seung-Ha Oh
exaly  

Genotype–phenotype correlations for SLC26A4-related deafness

Human Genetics, 2007
Tao Yang, Hela Azaiez, Richard J Smith
exaly  

Association of SLC26A4 mutations, morphology, and hearing in pendred syndrome and NSEVA

Laryngoscope, 2019
Nanna Dahl Rendtorff, Per Cayé-Thomasen, Kristianna Mey   +2 more
exaly  

A systematic review and meta-analysis of common mutations of SLC26A4 gene in Asian populations

International Journal of Pediatric Otorhinolaryngology, 2013
Yufen Guo, Xiaowen Liu, Wan Du
exaly  

Hypo-Functional SLC26A4 variants associated with nonsyndromic hearing loss and enlargement of the vestibular aqueduct: Genotype-phenotype correlation or coincidental polymorphisms?†

Human Mutation, 2009
Byung Yoon Choi, John A. Butman, Andrew J Griffith   +2 more
exaly  

Subgroups of enlarged vestibular aqueduct in relation to SLC26A4 mutations and hearing loss

Laryngoscope, 2014
Tatsuo Matsunaga, Atsuko Nakano, Hideki Mutai   +2 more
exaly  

SLC26A4 mutation spectrum associated with DFNB4 deafness and Pendred's syndrome in Pakistanis

Journal of Human Genetics, 2009
Andrew J Griffith, Zubair M Ahmed, Thomas B. Friedman   +2 more
exaly