Patterns and distribution of de novo mutations in multiplex Middle Eastern families حسب Muhammad Kohailan (748774)

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A loss-of-function AGTR1 variant in a critically-ill infant with renal tubular dysgenesis: case presentation and literature review حسب Aljazi Al-Maraghi (14056975)

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Integrating Genome Sequencing and Untargeted Metabolomics in Monozygotic Twins with a Rare Complex Neurological Disorder حسب Rulan Shaath (17112852)

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Genomic architecture of autism spectrum disorder in Qatar: The BARAKA-Qatar Study حسب Mona Abdi (10196665)

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