Items where Author is "Fazel-Najafabadi, E."

Article

(2016) Genomic rearrangement screening of the BRCA1 from seventy Iranian high-risk breast cancer families. Journal of Research in Medical Sciences. ISSN 1735-1995

(2015) Detection of Intragenic SMN1 Mutations in Spinal Muscular Atrophy Patients With a Single Copy of SMN1. Journal of Child Neurology. pp. 558-562. ISSN 0883-0738

(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) Structural and functional impact of missense mutations in TPMT: An integrated computational approach. Computational Biology and Chemistry. pp. 48-55. ISSN 1476-9271

(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