Author = Morteza Hashemzadeh Chaleshtori
Number of Articles: 3
Contribution of GJB2 Mutations and Four Common DFNB Loci in Autosomal Recessive Non-Syndromic Hearing Impairment in Markazi and Qom Provinces of Iran

Volume 7, Issue 2, April 2009, Pages 108-111

Abdorrahim Sadeghi; Mohammad Hossein Sanati; Fatemeh Alasti; Morteza Hashemzadeh Chaleshtori; Saeid Mahmoudian; Mitra Ataei

Mutation analysis of connexin 26 gene and del(GJB6-D13S1830) in patients with hereditary deafness from two provinces in Iran

Volume 3, Issue 4, October 2005, Pages 255-258

Abdorrahim Sadeghi; Mohammad Hossein Sanati; Fatemeh Alasti; Morteza Hashemzadeh Chaleshtori; Mitra Ataei

Association of Apolipoprotein E Polymorphism with Susceptibility to Multiple Sclerosis

Volume 2, Issue 1, January 2004, Pages 49-54

Valeh Hadavi; Mohammad H Sanati; Daroush Farhud; Masoud Hushmand; Morteza Hashemzadeh Chaleshtori; Seyed Masoud Nabavi; Masoud Younesian; Maziar Seyedian

Iranian Journal of Biotechnology

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