Items where Author is "Haghighat-Nia, A."

Article

(2015) Mutation spectrum of autosomal recessive non-syndromic hearing loss in central Iran. International Journal of Pediatric Otorhinolaryngology. pp. 1892-1895. ISSN 0165-5876

(2015) A new compound heterozygous mutation in GJB2 causes nonsyndromic hearing loss in a consanguineous Iranian family. International Journal of Pediatric Otorhinolaryngology. pp. 553-556. ISSN 0165-5876