SMN1 and NAIP genes deletions in different types of spinal muscular atrophy in Khuzestan province, Iran.Published in:Medical Journal of the Islamic Republic of Iran, 2011, v. 25, n. 4, p. 216By:Nezhad, Seyed Reza Kazemi;Mosavi, Fatemeh;Galehdari, Ali Akbar Momen Hamid;Mohamadian, GholamrezaPublication type:Article
Identification of a novel de novo mutation in the NIPBL gene in an Iranian patient with Cornelia de Lange syndrome: A case report.Published in:2011By:Galehdari, Hamid;Monajemzadeh, Roya;Nazem, Habibolah;Mohamadian, Gholamreza;Pedram, MohammadPublication type:journal article