E. Nikkhah

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

R. Safaralizadeh, M. H. Hosseinpour Feizi, N. Golchin, 2018, Cell journal.

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

H. Galehdari, A. Foroughmand, E. Nikkhah, 2015, Cell journal.