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Haifa Mansour

Showing results (1-10 of 3) with videos related to

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Frontiers in Pediatrics|March 3, 2022
Genome-Wide Association Study-Guided Exome Rare Variant Burden Analysis Identifies IL1R1 and CD3E as Potential Autoimmunity Risk Genes for Celiac DiseaseHaifa Mansour, Babajan Banaganapalli, Khalidah Khalid Nasser, et al.
Annals of Saudi Medicine|April 6, 2017
A novel WDR62 mutation causes primary microcephaly in a large consanguineous Saudi familyMuhammad Imran Naseer, Mahmood Rasool, Sameera Sogaty, et al.
Scientific Reports|October 2, 2020
Exploring celiac disease candidate pathways by global gene expression profiling and gene network cluster analysisBabajan Banaganapalli, Haifa Mansour, Arif Mohammed, et al.
Pageof 1

Showing results (1-10 of 3) with videos related to

Sort By:
Pageof 1
Frontiers in Pediatrics|March 3, 2022
Genome-Wide Association Study-Guided Exome Rare Variant Burden Analysis Identifies IL1R1 and CD3E as Potential Autoimmunity Risk Genes for Celiac DiseaseHaifa Mansour, Babajan Banaganapalli, Khalidah Khalid Nasser, et al.
Annals of Saudi Medicine|April 6, 2017
A novel WDR62 mutation causes primary microcephaly in a large consanguineous Saudi familyMuhammad Imran Naseer, Mahmood Rasool, Sameera Sogaty, et al.
Scientific Reports|October 2, 2020
Exploring celiac disease candidate pathways by global gene expression profiling and gene network cluster analysisBabajan Banaganapalli, Haifa Mansour, Arif Mohammed, et al.
Pageof 1