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Nature Communications|February 24, 2021
Whole genome sequencing in the Middle Eastern Qatari population identifies genetic associations with 45 clinically relevant traitsGaurav Thareja, Yasser Al-Sarraj, Aziz Belkadi, et al.
Frontiers in Nutrition|October 16, 2023
Genetic determinants of Vitamin D deficiency in the Middle Eastern Qatari population: a genome-wide association studyNagham Nafiz Hendi, Yasser Al-Sarraj, Umm-Kulthum Ismail Umlai, et al.
Clinical Case Reports|December 17, 2016
Mosaic partial pericentromeric trisomy 8 and maternal uniparental disomy in a male patient with autism spectrum disorderDina F Ahram, Danae Stambouli, Aleksandra Syrogianni, et al.
Genes|March 28, 2026
Characterization of a Familial Goldenhar Syndrome Case Using Whole-Exome SequencingYosra Bejaoui, Yasser Al-Sarraj, Jana Al-Hage, et al.
Clinical Case Reports|January 24, 2015
Distal trisomy 10q syndrome, report of a patient with duplicated q24.31 - qter, autism spectrum disorder and unusual featuresYasser Al-Sarraj, Hakam Abu Al-Khair, Rowaida Ziad Taha, et al.
Clinical Case Reports|June 8, 2017
A chromosomal microdeletion of 15q in a female patient with epilepsy, ID, and autism spectrum disorder: a case reportDina F Ahram, Yasser Al-Sarraj, Rowaida Z Taha, et al.
Genes|June 2, 2021
Family-Based Genome-Wide Association Study of Autism Spectrum Disorder in Middle Eastern FamiliesYasser Al-Sarraj, Eman Al-Dous, Rowaida Z Taha, et al.
International Journal of Molecular Sciences|January 8, 2023
The Genetic Spectrum of Maturity-Onset Diabetes of the Young (MODY) in Qatar, a Population-Based StudyAsma A Elashi, Salman M Toor, Ilhame Diboun, et al.
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