Showing 1 - 4 results of 4 for search 'H Najmabadi', query time: 0.02s Refine Results
  1. 1
    Detection of Rare and Unknown Mutations in ß- tathalassemia Traits in Iran

    Detection of Rare and Unknown Mutations in ß- tathalassemia Traits in Iran by M Habibi Roudknar, H Najmabadi, P Derakhshandeh, DD Farhud

    Published 2003
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  2. 2
    Detection of Rare and Unknown Mutations in ß- tathalassemia Traits in Iran

    Detection of Rare and Unknown Mutations in ß- tathalassemia Traits in Iran by M Habibi Roudknar, H Najmabadi, P Derakhshandeh, DD Farhud

    Published 2003
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  3. 3
    "Molecular Analysis of Iranian Patients with Duchenne/Becker Muscular Dystrophies"

    "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
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  4. 4
    "Molecular Analysis of Iranian Patients with Duchenne/Becker Muscular Dystrophies"

    "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
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