1. Novel Mutation in LARP7 in Two Iranian Consanguineous Families with Syndromic Intellectual Disability and Facial Dysmorphism

Goli Kazemi , Fatemeh Peymani, Marzieh Mohseni, Farzane Zare Ashrafi, Sanaz Arzhangi, Fariba Ardalani, Fatemeh Aghakhani Moghaddam, Kimia Kahrizi, Hossein Najmabadi*

Arch Iran Med. 2020;23(12): 842-847. doi: 10.34172/aim.2020.112

Scopus ID: 85097789447

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2. Characterizing Genotypes and Phenotypes Associated with Dysfunction of Channel-Encoding Genes in a Cohort of Patients with Intellectual Disability

Naeim Ehtesham , Meysam Mosallaei, Maryam Beheshtian , Shahrouz Khoshbakht, Mahsa Fadaee, Raheleh Vazehan, Mehrshid Faraji Zonooz, Parvaneh Karimzadeh , Kimia Kahrizi, Hossein Najmabadi*

Arch Iran Med. 2022;25(12): 788-797. doi: 10.34172/aim.2022.124

PMCID: PMC10685845 PMID: 37543906

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A Monthly Peer-Reviewed Medical Journal Published by the Academy of Medical Sciences of the I.R. Iran; Indexed in PubMed/MEDLINE, ISI Web of Science, EMBASE, SCOPUS, CINHAL, PASCAL, CSA, SID, ISSN: Print 1029-2977, Online 1735-3947.The impact factor of Archives of Iranian Medicine according to Journal Citation Reports® (JCR®) 2016 is 1.20.