Cohen syndrome and early-onset epileptic encephalopathy in male triplets: two disease-causing mutations in VPS13B and NAPB حسب Alice AbdelAleem (17753799)

"…Sanger sequencing verified the segregation of the two recessive gene variants with the phenotype in family members. The prediction algorithms support the pathogenicity of these variants. …"

Decision-level Gait Fusion for Human Identification at a Distance حسب Al-Tayyan, Amer

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Copy number variations in the genome of the Qatari population حسب Khalid A. Fakhro (3158862)

"…<p>The populations of the Arabian Peninsula remain the least represented in public genetic databases, both in terms of single nucleotide variants and of larger genomic mutations. …"