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Quoted phrase not found in phrase index: "Autosomal recessive nonsyndromic hearing loss 12"
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Improving the Management of Patients with Hearing Loss by the Implementation of an NGS Panel in Clinical Practice.
García-García G, Berzal-Serrano A, García-Díaz P, Villanova-Aparisi R, Juárez-Rodríguez S, de Paula-Vernetta C, Cavallé-Garrido L, Jaijo T, Armengot-Carceller M, Millán JM, Aller E. García-García G, et al. Genes (Basel). 2020 Dec 7;11(12):1467. doi: 10.3390/genes11121467. Genes (Basel). 2020. PMID: 33297549 Free PMC article. Clinical Trial.
A cohort of 128 patients from 118 families diagnosed with non-syndromic or syndromic hearing loss (HL) underwent an exhaustive clinical evaluation. Molecular analysis was performed using targeted next-generation sequencing (NGS) with a custom panel that included 59 genes a …
A cohort of 128 patients from 118 families diagnosed with non-syndromic or syndromic hearing loss (HL) underwent an exhaustive clinical …
Genotyping data and novel haplotype diversity of STR markers in the SLC26A4 gene region in five ethnic groups of the Iranian population.
Mojtabavi Naeini M, Mesrian Tanha H, Hashemzadeh Chaleshtori M, Vallian S. Mojtabavi Naeini M, et al. Genet Test Mol Biomarkers. 2014 Dec;18(12):820-5. doi: 10.1089/gtmb.2014.0178. Genet Test Mol Biomarkers. 2014. PMID: 25390158 Free PMC article. Clinical Trial.
BACKGROUND AND AIMS: SLC26A4 gene mutations are the second currently identifiable genetic cause of autosomal recessive nonsyndromic hearing loss after GJB2 mutations. ...
BACKGROUND AND AIMS: SLC26A4 gene mutations are the second currently identifiable genetic cause of autosomal recessive nons …