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Cureus|April 19, 2023
Haptic Amputation Under Endoscopic Guidance in Uveitis-Glaucoma-Hyphema Syndrome: A Case ReportMerai Alshehri, Ali Al Beshri, Dania BameflehCalcified Tissue International|February 11, 2020
Fragile Bones Secondary to SMURF1 Gene DuplicationRawan Al-Rawi, Ali Al-Beshri, Fady M Mikhail, et al.American Journal of Medical Genetics. Part A|December 2, 2024
Constitutional Mosaic Pericentromeric Trisomy 8 in a Female Patient With Aplastic AnemiaMin Gao, Yunjia Chen, Pongtawat Lertwilaiwittaya, et al.Diagnostics (Basel, Switzerland)|August 23, 2020
An Adoptive Threshold-Based Multi-Level Deep Convolutional Neural Network for Glaucoma Eye Disease Detection and ClassificationMuhammad Aamir, Muhammad Irfan, Tariq Ali, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 20, 2023
DLG2 intragenic exonic deletions reinforce the link to neurodevelopmental disorders and suggest a potential association with congenital anomalies and dysmorphismYunjia Chen, Ender Karaca, Nathaniel H Robin, et al.Human Mutation|December 1, 2020
Mitochondrial genome variant m.3250T>C as a possible risk factor for mitochondrial cardiomyopathyTeresa Campbell, Xiaoting Lou, Jesse Slone, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 27, 2020
The broad phenotypic spectrum of PPP2R1A-related neurodevelopmental disorders correlates with the degree of biochemical dysfunctionLisa Lenaerts, Sara Reynhout, Iris Verbinnen, et al.Pageof 1