Different Types of the Coagulation Disorders in Hamadan and A Comparison of the ABO & Rh Blood Group Distribution in the Patients and the Control Group by Hamid Pour-Jafari, Morteza Hashemzadeh Chaleshtori

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Expandable DNA Repeat and Human Hereditary Disorders by Shahin Ramazi, Ali Fasihi, Maryam Godarziyan, Morteza Hashemzadeh-Chaleshtori

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Population Data on D7S2425 Marker in Five Ethnic Groups of the Iranian Population: A Highly Informative Marker for Molecular Diagnosis of ARNSHL by Marjan Mojtabavi Naeini, Sadeq Vallian Boroujeni, Morteza Hashemzadeh Chaleshtori

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Screening of Myo7A Mutations in Iranian Patients with Autosomal Recessive Hearing Loss from West of Iran by Samira ASGHARZADE, Somayeh REIISI, Mohammad Amin TABATABAIEFAR, Morteza HASHEMZADEH CHALESHTORI

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Clinical Aspects of Microsatellite Instability Testing in Colorectal Cancer by Mehrdad Zeinalian, Morteza Hashemzadeh-Chaleshtori, Rasoul Salehi, Mohammad Hassan Emami

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Mesenchymal stem cells versus their conditioned medium in the treatment of ischemia/reperfusion injury: Evaluation of efficacy and hepatic specific gene expression in mice by Somayeh Khosravi-Farsani, Arash Zaminy, Sedigheh Kazemi, Morteza Hashemzadeh-Chaleshtori

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Lack of Association between ESR1 and CYP1A1 Gene Polymorphisms and Susceptibility to Uterine Leiomyoma in Female Patients of Iranian Descent by Fatemeh Taghizade Mortezaee, Mohammad Amin Tabatabaiefar, Morteza Hashemzadeh Chaleshtori, Sepideh Miraj

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Tumor microsatellite instability and clinicopathologic features in Iranian colorectal cancer patients at risk for Lynch syndrome by Mehrdad Zeinalian, Morteza Hashemzadeh-Chaleshtori, Rasoul Salehi, Mohammad Kazemi, Mohammad Hassan Emami

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Familial Colorectal CancerType X in Central Iran: A New Clinicopathologic Description by Mehrdad Zeinalian, Mahdi Hadian, Morteza Hashemzadeh-Chaleshtori, Rasoul Salehi, Mohammad Hassan Emami

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بررسی جهش‌های ژن LRTOMT (لوکوس 63DFNB) در بیماران مبتلا به ناشنوایی غیر سندرمیک مغلوب استان هرمزگان با استفاده از روش‌های PCR-SSCP، PCR-HA و توالی‌یابی DNA... by Shahrbanoo Parchami-Barjui, Somayeh Reiisi, Fatemeh Rezaiean, Fatemeh Heybati, Morteza Hashemzadeh-Chaleshtori

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Novel MYO15A variants are associated with hearing loss in the two Iranian pedigrees by Somayeh Khatami, Masomeh Askari, Fatemeh Bahreini, Morteza Hashemzadeh-Chaleshtori, Saeed Hematian, Samira Asgharzade

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Investigation of Mutations in Exons 15 and 18 of MYBPC3 Gene in Hypertrophic Cardiomyopathy Patients by Behnaz Sadat Abedi, Seyedeh Zohreh kiyani, Morteza Hashemzadeh Chaleshtori, Shahrbanoo Parchami, Abbas Doosti

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Molecular Mechanisms behind Free Radical Scavengers Function against Oxidative Stress by Fereshteh Ahmadinejad, Simon Geir Møller, Morteza Hashemzadeh-Chaleshtori, Gholamreza Bidkhori, Mohammad-Saeid Jami

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تجزیه و تحلیل پیوستگی ژنتیکی لوکوس‌های DFNB40 و DFNB48 در خانواده‌هایی با ناشنوایی غیر سندرمی مغلوب اتوزومی از استان‌های غربی کشور... by Azam Pourahmadiyan, Mohammad Amin Tabatabaiefar, Somayeh Reiisi, Paria Alipour, Najmeh Fattahi, Morteza Hashemzadeh-Chaleshtori

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Increased levels of miR-124 in human dental pulp stem cells alter the expression of neural markers by Ameneh Mehri-Ghahfarrokhi, Zahra Pourteymourfard-Tabrizi, Effat Farrokhi, Morteza Hashemzadeh Chaleshtori, Mohammad-Saeid Jami

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Molecular genetic study in a cohort of Iranian families suspected to maturity-onset diabetes of the young, reveals a recurrent mutation and a high-risk variant in the CEL gene by Akram Sarmadi, Aliasgar Mohammadi, Fatemeh Tabatabaei, Zahra Nouri, Morteza Hashemzadeh Chaleshtori, Mohammad Amin Tabatabaiefar

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A Simple, Rapid, and Efficient Method for Isolating Mesenchymal Stem Cells from the Entire Umbilical Cord by Mehdi Banitalebi Dehkordi, Zahra Madjd, Morteza Hashemzadeh Chaleshtori, Reza Meshkani, Laleh Nikfarjam, Abdol-Mohammad Kajbafzadeh

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Evaluation of response to hepatitis B vaccine in iranian 6–18-year-old students by Alizamen Salehifard Jouneghani, Morteza Hashemzadeh Chaleshtori, Abolfazl Khoshdel, Soleiman Kheiri, Effat Farrokhi, Pooran Khalafian, Zahra Aliyari

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Compound Heterozygosity for Two Novel Mutations in a Large Iranian Pedigree with Pendred Syndrome by Nasrin Yazdanpanahi, Mohammad Amin Tabatabaiefar, Effat Farrokhi, Narges Abdian, Nader Bagheri, Shirin Shahbazi, Zahra Noormohammadi, Morteza Hashemzadeh Chaleshtori

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Screening of 10 DFNB Loci Causing Autosomal Recessive Non-Syndromic Hearing Loss in Two Iranian Populations Negative for GJB2 Mutations by Mahbobeh KOOHIYAN, Somayeh REIISI, Fatemeh AZADEGAN-DEHKORDI, Mansoor SALEHI, Hamidreza ABTAHI, Morteza HASHEMZADEH-CHALESHTORI, Mohammad Reza NOORI-DALOII, Mohammad Amin TABATABAIEFAR

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