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International Journal of Cancer|May 9, 2020
Error-prone DNA repair pathways as determinants of immunotherapy activity: an emerging scenario for cancer treatmentDaniele Caracciolo, Caterina Riillo, Mariamena Arbitrio, et al.
Frontiers in Psychiatry|December 20, 2021
Delineating the Relationships Between Motor, Cognitive-Executive and Psychiatric Symptoms in Female FMR1 Premutation CarriersDarren R Hocking, Danuta Z Loesch, Paige Stimpson, et al.
Annals of Surgery|July 30, 2014
The Use of Caffeinated Substances by Surgeons for Cognitive EnhancementAndreas G Franke, Christiana Bagusat, Carolyn McFarlane, et al.
BMC Medical Genetics|October 15, 2014
Mapping the deletion endpoints in individuals with 22q11.2 deletion syndrome by droplet digital PCRVicki J Hwang, Dianna Maar, John Regan, et al.
European Journal of Medical Genetics|December 2, 2017
A higher rare CNV burden in the genetic background potentially contributes to intellectual disability phenotypes in 22q11.2 deletion syndromeMatthew Jensen, R Frank Kooy, Tony J Simon, et al.
Frontiers in Genetics|September 14, 2018
Impact ofEleonora Napoli, Andrea Schneider, Randi Hagerman, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|November 11, 2009
Insulin resistance is not coupled with defective insulin secretion in primary hyperparathyroidismF Tassone, M Procopio, L Gianotti, et al.
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