Hasil Pencarian - Huda Alajlan

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  1. 1
    A unique STK4 mutation truncating only the C-terminal SARAH domain results in a mild clinical phenotype despite severe T cell lymphopenia: Case report

    A unique STK4 mutation truncating only the C-terminal SARAH domain results in a mild clinical phenotype despite severe T cell lymphopenia: Case report oleh Bandar Al-Saud, Bandar Al-Saud, Huda Alajlan, Hibah Alruwaili, Latifa Almoaibed, Amer Al-Mazrou, Hazem Ghebeh, Hazem Ghebeh, Monther Al-Alwan, Monther Al-Alwan, Anas M. Alazami

    Diterbitkan 2024-02-01
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  2. 2
    Novel CARMIL2 Mutations in Patients with Variable Clinical Dermatitis, Infections, and Combined Immunodeficiency

    Novel CARMIL2 Mutations in Patients with Variable Clinical Dermatitis, Infections, and Combined Immunodeficiency oleh Anas M. Alazami, Anas M. Alazami, Maryam Al-Helale, Safa Alhissi, Bandar Al-Saud, Huda Alajlan, Dorota Monies, Dorota Monies, Zeeshan Shah, Zeeshan Shah, Mohamed Abouelhoda, Mohamed Abouelhoda, Rand Arnaout, Rand Arnaout, Hasan Al-Dhekri, Nouf S. Al-Numair, Hazem Ghebeh, Hazem Ghebeh, Farrukh Sheikh, Hamoud Al-Mousa, Hamoud Al-Mousa, Hamoud Al-Mousa

    Diterbitkan 2018-02-01
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