Items where Author is "Azadegan-Dehkordi, Fatemeh"

Up a level
Export as [feed] Atom [feed] RSS 1.0 [feed] RSS 2.0
Group by: Item Type | No Grouping
Jump to: Article
Number of items: 8.

Article

Koohiyan, Mahbobeh and Koohian, Farideh and Azadegan-Dehkordi, Fatemeh (2020) GJB2-related hearing loss in central Iran: Review of the spectrum and frequency of gene mutations. Annals of Human Genetics, 84 (2). ISSN 00034800

Koohiyan, Mahbobeh and Azadegan-Dehkordi, Fatemeh and Koohian, Farideh and Hashemzadeh-Chaleshtori, Morteza (2019) Genetics of Hearing Loss in North Iran Population: An Update of Spectrum and Frequency of GJB2 Mutations. JOURNAL OF AUDIOLOGY AND OTOLOGY.

Koohiyan, Mahbobeh and Koohian, Farideh and Azadegan-Dehkordi, Fatemeh (2019) GJB2-related hearing loss in central Iran: Review of the spectrum and frequency of gene mutations. ANNALS OF HUMAN GENETICS.

Koohiyan, Mahboobeh and Reiisi, Somayeh and Azadegan-Dehkordi, Fatemeh and Salehi, Mansour and Abtahi, Hamidreza and Hashemzadeh-Chaleshtori, Morteza and Noori-Daloii, Mohammad Reza and Tabatabaiefar, Mohammad Amin (2019) Screening of 10 DFNB Loci Causing Autosomal Recessive Non-Syndromic Hearing Loss in Two Iranian Populations Negative for GJB2 Mutations. Iranian Journal of Public Health. ISSN 2251-6085

Koohiyan, Mahbobeh and Azadegan-Dehkordi, Fatemeh and Koohian, Farideh and Abolhasani, Marziye and Hashemzadeh-Chaleshtori, Morteza (2019) Genetics of hereditary hearing loss in east Iran population: A systematic review of GJB2 mutations. INTRACTABLE & RARE DISEASES RESEARCH.

Azadegan-Dehkordi, Fatemeh and Bahrami, Tayyebe and Shirzad, Maryam and Karbasi, Gelareh and Yazdanpanahi, Nasrin and Farrokhi, Effat and Koohiyan, Mahbobeh and Tabatabaiefar, Mohammad Amin and Hashemzadeh-Chaleshtori, Morteza (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 & Otology. ISSN 2384-1621

Azadegan-Dehkordi, Fatemeh and Koohiyan, Mahbobeh and Shirzad, Maryam and Bahrami, Tayyeb and Yazdanpanahi, Nasrin and Tabatabaiefar, MohammadAmin and Pourpaknia, Reza and Farrokhi, Effat and Hashemzadeh-Chaleshtori, Morteza (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, 25 (2). p. 97. ISSN 0971-7749

Azadegan-Dehkordi, Fatemeh and Ahmadi, Reza and Koohiyan, Mahbobeh and Hashemzadeh-Chaleshtori, Morteza (2019) Update of spectrum c.35delG and c.-23+1G>A mutations on theGJB2gene in individuals with autosomal recessive nonsyndromic hearing loss. Annals of Human Genetics, 83 (1). pp. 1-10. ISSN 00034800

This list was generated on Tue Aug 4 01:17:24 2020 IRDT.