Showing 1 - 6 results of 6 for search 'H. Najmabadi', query time: 0.03s
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Detection of Rare and Unknown Mutations in ß- tathalassemia Traits in Iran by M Habibi Roudknar, H Najmabadi, P Derakhshandeh, DD Farhud
Published 2003-06-01
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PREVALENCE OF Y CHROMOSOME MICRODELETIONS IN IRANIAN INFERTILE MEN by F. Akbari Asbagh, A. Sina, H. Najmabadi, M. T. Akbari, A. Tabarroki Gh. Pourm
Published 2003-09-01
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PREVALENCE OF Y CHROMOSOME MICRODELETIONS IN IRANIAN INFERTILE MEN by F. Akbari Asbagh, A. Sina, H. Najmabadi, M. T. Akbari, A. Tabarroki Gh. Pourm
Published 2003-07-01
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"Molecular Analysis of Iranian Patients with Duchenne/Becker Muscular Dystrophies" by S Kheradmand kia, DD Farhud, S Zeinali, AR Mowjoodi, H Najmabadi, F Pourfarzad, P Derakhshandeh
Published 2003-09-01
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Relative Frequency of 35delG Mutation in GJB2 Gene in Autosomal Recessive Non-Syndromic Hearing Loss (ARNSHL) Patients in Kerman Population by N Bazazzadegan, N Mirhoseini, H Ziaaddini, AR Asadi, K Kahrizi, S Arzhangi, A Astani, M Mohseni, Y Riazalhosseini, M Nejat, Kh Jalalvand, RJH Smith, C Nishimura, H Najmabadi
Published 2004-07-01
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