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Banitalebi, Golandam. and Montazerzohor, Mostafa. and Farrokhi, Effat. and Abolhasani, Marzieh. and Reissi, Somayeh. and Heydari, Soraya. and Ataii, Zohreh. and Azadegan-Dehkordi, Fatemeh. and Hoseinipoor, Azam. and Hashemzadeh-Chaleshtori, Morteza. (2012) Study of three common mitochondrial mutations in Arab patients with nonsyndromic hearing loss in Khuzestan province, I.R.Iran. Journal of Shahrekord Uuniversity of Medical Sciences, 14.
Hashemzadeh-Chaleshtori, Morteza. and Akbari, mohammad taghi. and Khazraei, Hamid. and Abolhasani, Marzieh. and Reisi, Somayeh and Ataei, Zohreh. and Saedi-Marghmaleki, Mojtaba. and Shirmardi, Seyed Abolfath. and Farrokhi, Effat. and Montazer Zohouri, Mostafa and Azadegan-Dehkordi, Fatemeh. (2011) Screening of three common mtDNA mutations among subjects with autosomal recessive non-syndromic hearing loss in Sistan va Baluchestan province, Iran. Zahedan Journal of Research in Medical Sciences, 13 (5).
Hashemzadeh-Chaleshtori, Morteza. and Banitalebi, Golandam. and Reisi, Somayeh and Azadegan-Dehkordi, Fatemeh. and Abolhasani, Marzieh. and Ghasemi, Soraya. and Shirmardi, Seyed Abolfath. and Farrokhi, Effat. and Taherzadeh Ghahfarrokhi, Maryam. (2010) DFNB59 Gene Mutations and its Association with Deafness in Schoolchildren in Kohgilooyeh & Boyerahmad Province. Armaghane danesh, 14 (4).
