1. A Rare Cytogenetic Variant of Monosomy 18p Syndrome as a Consequence of Whole-Arm Translocation between Chromosomes 13 and 18

Moeinadin Safavi*, Mohammad Taghi Haghi Ashtiani, Reza Shervin Badv, Aileen Azari-Yam, Mohammad Vasei*

Arch Iran Med. 2019;22(10): 627-628.

PMID: 31679365 Scopus ID: 85074411286

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Case Report

2. A Patient with Trisomy 4p and Monosomy 10q

Maryam Sobhani, Parisa Tahmasbi, Fatemeh Nasiri, Mitra Rahnama, Roxana Karimi-Nejad, Mohammad Amin Tabatabaiefar*

Arch Iran Med. 2019;22(7): 414-417.

PMID: 31679386 Scopus ID: 85071361599

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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.