Showing results (1-10 of 30) with videos related to

Sort By:
Pageof 3
Genes|February 25, 2022
Consanguinity and Congenital Heart Disease Susceptibility: Insights into Rare Genetic Variations in Saudi ArabiaNour Albesher, Salam Massadeh, Sabah M Hassan, et al.
Analytical and Bioanalytical Chemistry|September 17, 2009
Electrophoretic properties of BSA-coated quantum dotsWendelin Bücking, Salam Massadeh, Alexei Merkulov, et al.
Journal of Epidemiology and Global Health|January 3, 2022
Correlation between ABO Blood Group Phenotype and the Risk of COVID-19 Infection and Severity of Disease in a Saudi Arabian CohortDunia Jawdat, Ali Hajeer, Salam Massadeh, et al.
Journal of Medical Genetics|February 2, 2017
A missense mutation in the CRBN gene that segregates with intellectual disability and self-mutilating behaviour in a consanguineous Saudi familyAtia Sheereen, Manal Alaamery, Shahad Bawazeer, et al.
Journal of Medical Case Reports|May 7, 2026
Jagged-1 mutation is associated with congenital heart defects: a case reportOthman Alahmed, Manal Alaamery, Fahad Alhabshan, et al.
Clinical Genetics|April 15, 2020
PDCD6IP, encoding a regulator of the ESCRT complex, is mutated in microcephalyAmjad Khan, Manal Alaamery, Salam Massadeh, et al.
Clinical Immunology (Orlando, Fla.)|December 20, 2021
Association of KIR gene polymorphisms with COVID-19 diseaseAli Hajeer, Dunia Jawdat, Salam Massadeh, et al.
Journal of Infection and Public Health|August 22, 2024
Association between human leukocyte antigen alleles and COVID-19 disease severityAli Hajeer, Dunia Jawdat, Salam Massadeh, et al.
Pageof 3