Items where Author is "Bahrami, T."

(2019) Mutation Analysis of GJB2 and GJB6 Genes and Screening of Nine Common DFNB Loci in Iranian Pedigrees with Autosomal Recessive Nonsyndromic Hearing Loss. Indian Journal of Otology. pp. 97-102. ISSN 0971-7749

(2019) Mutations in GJB2 as Major Causes of Autosomal Recessive Non-Syndromic Hearing Loss: First Report of c.299-300delAT Mutation in Kurdish Population of Iran. Journal of Audiology and Otology. pp. 20-26. ISSN 2384-1621

(2018) A novel variant of SLC26A4 and first report of the c.716T > A variant in Iranian pedigrees with non-syndromic sensorineural hearing loss. American Journal of Otolaryngology. pp. 719-725. ISSN 0196-0709

(2017) A Novel Pathogenic Variant in the MITF Gene Segregating with a Unique Spectrum of Ocular Findings in an Extended Iranian Waardenburg Syndrome Kindred. Molecular Syndromology. pp. 195-200. ISSN 1661-8769

(2015) Molecular and clinical characterization of Waardenburg syndrome type I in an Iranian cohort with two novel PAX3 mutations. Gene. pp. 302-307. ISSN 0378-1119

(2015) A novel mutation in the PAX3 gene causes Waardenburg syndrome type I in an Iranian family. International Journal of Pediatric Otorhinolaryngology. pp. 1736-1740. ISSN 0165-5876