Search Results - Morad Khayat

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    Desmoglein 4 Mutation Underlies Autosomal Recessive Keratosis Pilaris Atrophicans by Eran Cohen-Barak, Nada Danial-Farran, Helwa Hammad, Ola Aleme, Judith Krauz, Ester Gavish, Morad Khayat, Michael Ziv, Stavit Shalev

    Published 2018
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    A Novel Homozygous Missense Variant in the LRRC32 Gene Is Associated With a New Syndrome of Cleft Palate, Progressive Vitreoretinopathy, Growth Retardation, and Developmental Delay by Zufit Hexner-Erlichman, Boris Fichtman, Yoav Zehavi, Yoav Zehavi, Morad Khayat, Haneen Jabaly-Habib, Haneen Jabaly-Habib, Lee S. Izhaki-Tavor, Moshe Dessau, Orly Elpeleg, Ronen Spiegel, Ronen Spiegel

    Published 2022
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