Search Results - "Nikkhah, Emad"

Identification of A Novel Compound Heterozygous Mutation in BBS12 in An Iranian Family with Bardet-Biedl Syndrome Using Targeted Next Generation Sequencing by Nikkhah, Emad, Safaralizadeh, Reza, Mohammadiasl, Javad, Tahmasebi Birgani, Maryam, Hosseinpour Feizi, Mohammad Ali, Golchin, Neda

“…Bardet-Biedl syndrome (BBS) is a pleiotropic and multisystemic disorder characterized by rod-cone dystrophy, polydactyly, learning difficulties, renal…”
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Association Study between Coronary Artery Disease and rs1333049 and rs10757274 Polymorphisms at 9p21 Locus in South-West Iran by Foroughmand, Ali Mohammad, Nikkhah, Emad, Galehdari, Hamid, Jadbabaee, Mohammad Hossin

“…Coronary artery disease (CAD) is a multi-factorial and heterogenic disease with atherosclerosis plaques formation in internal wall of coronary artery. Plaque…”
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Identification of A Novel Compound Heterozygous Mutation in BBS12 in An Iranian Family with Bardet-Biedl Syndrome Using Targeted Next Generation Sequencing by Nikkhah, Emad, Safaralizadeh, Reza, Mohammadiasl, Javad, Mohammad Ali Hosseinpour Feizi, Golchin, Neda

“…Bardet-Biedl syndrome (BBS) is a pleiotropic and multisystemic disorder characterized by rod-cone dystrophy, polydactyly, learning difficulties, renal…”
Get full text