يعرض 1 - 2 نتائج من 2 نتيجة بحث عن 'Tawfeg Ben‐Omran (14776975)', وقت الاستعلام: 0.01s تنقيح النتائج
  1. 1
    A founder RAB27A variant causes Griscelli syndrome type 2 with phenotypic heterogeneity in Qatari families

    A founder RAB27A variant causes Griscelli syndrome type 2 with phenotypic heterogeneity in Qatari families حسب Reem Al‐Sulaiman (14776948)

    منشور في 2020
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  2. 2
    Expanding on the phenotypic spectrum of Woodhouse‐Sakati syndrome due to founder pathogenic variant in <i>DCAF17</i>: Report of 58 additional patients from Qatar and literature review

    Expanding on the phenotypic spectrum of Woodhouse‐Sakati syndrome due to founder pathogenic variant in <i>DCAF17</i>: Report of 58 additional patients from Qatar and literature rev... حسب Rehab Ali (14152668)

    منشور في 2021
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