Association Study between Coronary Artery Disease and rs1333049 and rs10757274 Polymorphisms at 9p21 Locus in South-West Iran

por Foroughmand, Ali Mohammad, Nikkhah, Emad, Galehdari, Hamid, Jadbabaee, Mohammad Hossin
Publicado 2015

Identification of A Novel Compound Heterozygous Mutation in BBS12 in An Iranian Family with Bardet-Biedl Syndrome Using Targeted Next Generation Sequencing

por Nikkhah, Emad, Safaralizadeh, Reza, Mohammadiasl, Javad, Tahmasebi Birgani, Maryam, Hosseinpour Feizi, Mohammad Ali, Golchin, Neda
Publicado 2018