Hasil Pencarian - Mohammad Javad Ghorbani

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  1. 1
    Update on a previously reported missense mutation: The c.1160 C>A mutation in the UGT1A1 gene result in Crigler–Najjar syndrome type 1

    Update on a previously reported missense mutation: The c.1160 C>A mutation in the UGT1A1 gene result in Crigler–Najjar syndrome type 1 oleh Mohammad Javad Ghorbani, Seyed Mohsen Dehghani

    Diterbitkan 2021-11-01
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  2. 2
    Developing HSE Strategic Plan (Case study: Port and Maritime Organization)

    Developing HSE Strategic Plan (Case study: Port and Maritime Organization) oleh Moslem Alimohammadlou, Shabnam Shaker, Seyed-Hadi Mirghaderi, Majid Babolhavaeji, Mohammad-Javad Ghorbani

    Diterbitkan 2012-02-01
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  3. 3
    Evaluation of Genome in Early Familial Coronary Artery Disease: A Case Report

    Evaluation of Genome in Early Familial Coronary Artery Disease: A Case Report oleh Mohammad Javad Ghorbani, Nematollah Razmi, Seyed Mohammad Bagher Tabei, Mohammad Javad Zibaeenezhad, Hamid Reza Goodarzi

    Diterbitkan 2019-06-01
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  4. 4
    A substitution mutation in LRP8 gene is significantly associated with susceptibility to familial myocardial infarction

    A substitution mutation in LRP8 gene is significantly associated with susceptibility to familial myocardial infarction oleh Mohammad Javad Ghorbani, Nematollah Razmi, Seyed Mohammad Bagher Tabei, Mohammad Javad Zibaeenezhad, Hamid Reza Goodarzi

    Diterbitkan 2020-10-01
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