المشروعات في السنة
نتائج البحث
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نشط
Functional Characterization of biallelic mutations of Centrobin as causative of Seckel-like syndrome
١/١/٢٤ → ١٢/٣١/٢٥
المشروع: بحوث المنح الداخلية
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منتهي
Characterization of Hitherto Undiagnosed Adult Neurogenetic Disorders in Oman
٩/١/١٩ → ٨/٣١/٢١
المشروع: MoHERI
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Functional characterization of RYR3 mutations associated with neurodevelopment disorders.
١/١/١٩ → ١٢/٣١/٢٠
المشروع: بحوث المنح الداخلية
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Identifying Genetic causes of Autosomal Recessive Intellectual Disability
١/١/١٦ → ١٢/٣١/٢٠
المشروع: Consultancy project
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A new paradigm for the molecular diagnosis of uncharacterized genetic disorders in the Omani population
٩/١/١٤ → ٥/٣١/١٨
المشروع: MoHERI
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The genetics of cardiometabolic disorders among Arabs of Oman Family Study
٩/١/١٤ → ٨/٣١/١٧
المشروع: MoHERI
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Molecular epidemiology and diagnosis study of common inborn errors of metabolism disorders in Oman and UAE: Phase 2
١/١/١٤ → ١٢/٣١/١٤
المشروع: Other project