A preliminary study of inherited thrombophilic risk factors in different clinical manifestations of venous thromboembolism in central Iran

por Karimi, Ali, Abolhasani, Marziyeh, Hashemzadeh-Chaleshtori, Morteza, Pourgheysari, Batoul
Publicado 2015

Mutation Screening of Exons 7 and 13 of the TMC1 Gene in Autosomal Recessive Non-syndromic Hearing Loss (ARNSHL) in Iran

por Moradipour, Negar, Ghasemi-Dehkordi, Payam, Heibati, Fatemeh, Parchami-Barjui, Shahrbanuo, Abolhasani, Marziyeh, Rashki, Ahmad, Hashemzadeh-Chaleshtori, Morteza
Publicado 2016

Investigation of LRTOMT gene (locus DFNB63) mutations in Iranian patients with autosomal recessive non-syndromic hearing loss

por Taghizadeh, Seyyed Hossein, Kazeminezhad, Seyyed Reza, Sefidgar, Seyyed Ali Asghar, Yazdanpanahi, Nasrin, Tabatabaeifar, Mohammad Amin, Yousefi, Ahmad, Lesani, Seyyed Mohammad, Abolhasani, Marziyeh, Hashemzadeh Chaleshtori, Morteza
Publicado 2013