Hasil Pencarian - Haifa Mansour

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  1. 1
    Genome-Wide Association Study-Guided Exome Rare Variant Burden Analysis Identifies IL1R1 and CD3E as Potential Autoimmunity Risk Genes for Celiac Disease

    Genome-Wide Association Study-Guided Exome Rare Variant Burden Analysis Identifies IL1R1 and CD3E as Potential Autoimmunity Risk Genes for Celiac Disease oleh Haifa Mansour, Haifa Mansour, Babajan Banaganapalli, Babajan Banaganapalli, Khalidah Khalid Nasser, Khalidah Khalid Nasser, Khalidah Khalid Nasser, Jumana Yousuf Al-Aama, Jumana Yousuf Al-Aama, Noor Ahmad Shaik, Noor Ahmad Shaik, Omar Ibrahim Saadah, Omar Ibrahim Saadah, Ramu Elango, Ramu Elango

    Diterbitkan 2022-02-01
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  2. 2
    A novel WDR62 mutation causes primary microcephaly in a large consanguineous Saudi family

    A novel WDR62 mutation causes primary microcephaly in a large consanguineous Saudi family oleh Muhammad Imran Naseer, Mahmood Rasool, Sameera Sogaty, Rukhaa Adeel Chaudhary, Haifa Mansour Mansour, Adeel G. Chaudhary, Adel M. Abuzenadah, Mohammad H. Al-Qahtani

    Diterbitkan 2017-03-01
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