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American Journal of Human Genetics|December 1, 2001
Retinal dystrophy due to paternal isodisomy for chromosome 1 or chromosome 2, with homoallelism for mutations in RPE65 or MERTK, respectivelyDebra A Thompson, Christina L McHenry, Yun Li, et al.
The Protein Journal|November 8, 2025
Multi-scale In Silico and Biochemical Evaluation of Natural Bisbenzylisoquinoline Alkaloids as Aldose Reductase InhibitorsEmadeldin M Kamel, Noha A Ahmed, Sarah I Othman, et al.
Dentistry Journal|November 26, 2024
Histological Evaluation of Polyacid-Modified Composite Resin and Conventional Composite Resin Used for Primary Molars RestorationOmar A El Meligy, Hisham I Othman, Shahad N Abudawood, et al.
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