Works matching AU Ehlayel, Mohammad


Results: 17
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    Biallelic mutations in DNA ligase 1 underlie a spectrum of immune deficiencies.

    Published in:
    2018
    By:
    • Maffucci, Patrick;
    • Chavez, Jose;
    • Jurkiw, Thomas J.;
    • O'Brien, Patrick J.;
    • Abbott, Jordan K.;
    • Reynolds, Paul R.;
    • Worth, Austen;
    • Notarangelo, Luigi D.;
    • Felgentreff, Kerstin;
    • Cortes, Patricia;
    • Boisson, Bertrand;
    • Radigan, Lin;
    • Cobat, Aurélie;
    • Dinakar, Chitra;
    • Ehlayel, Mohammad;
    • Ben-Omran, Tawfeg;
    • Gelfand, Erwin W.;
    • Casanova, Jean-Laurent;
    • Cunningham-Rundles, Charlotte
    Publication type:
    journal article
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    A founder RAB27A variant causes Griscelli syndrome type 2 with phenotypic heterogeneity in Qatari families.

    Published in:
    American Journal of Medical Genetics. Part A, 2020, v. 182, n. 11, p. 2570, doi. 10.1002/ajmg.a.61829
    By:
    • Al‐Sulaiman, Reem;
    • Othman, Amna;
    • El‐Akouri, Karen;
    • Fareed, Shehab;
    • AlMulla, Hajer;
    • Sukik, Aseel;
    • Al‐Mureikhi, Mariam;
    • Shahbeck, Noora;
    • Ali, Rehab;
    • Al‐Mesaifri, Fatma;
    • Musa, Sara;
    • Al‐Mulla, Mariam;
    • Ibrahim, Khalid;
    • Mohamed, Khalid;
    • Al‐Nesef, Maryam Ali;
    • Ehlayel, Mohammad;
    • Ben‐Omran, Tawfeg
    Publication type:
    Article
    12

    Camel's milk allergy.

    Published in:
    Allergy & Asthma Proceedings, 2018, v. 39, n. 5, p. 384, doi. 10.2500/aap.2018.39.4150
    By:
    • Ehlayel, Mohammad;
    • Bener, Abdulbari
    Publication type:
    Article
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