Search Results - Labbaf, Afsaneh

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  1. 1
    Whole-exome sequencing identified a novel mutation of MLH1 in an extended family with lynch syndrome

    Whole-exome sequencing identified a novel mutation of MLH1 in an extended family with lynch syndrome by Ghaedi, Hamid, Ramsheh, Samira Molaei, Omidvar, Maryam Erfanian, Labbaf, Afsaneh, Alehabib, Elham, Akbari, Sanaz, Pourfatemi, Fatemeh, Darvish, Hossein

    Published in Genes & diseases
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  2. 2
    Association of miR-149 (RS2292832) Variant with the Risk of Coronary Artery Disease

    Association of miR-149 (RS2292832) Variant with the Risk of Coronary Artery Disease by Ghaffarzadeh, Maryam, Ghaedi, Hamid, Alipoor, Behnam, Omrani, Mir Davood, Kazerouni, Faranak, Shanaki, Mehrnoosh, Labbaf, Afsaneh, Pashaiefar, Hossein, Rahimipour, Ali

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