Showing results (251-260 of 408) with videos related to
Sort By:
Pageof 41
Journal of the European Academy of Dermatology and Venereology : JEADV|January 13, 2006
Effect of calcipotriol on epidermal cell populations in alefacept-treated psoriatic lesionsM W F M van Duijnhoven, J E M Körver, W H P M Vissers, et al.Human Mutation|July 30, 2013
Detection of clinically relevant copy number variants with whole-exome sequencingJoep de Ligt, Philip M Boone, Rolph Pfundt, et al.European Journal of Human Genetics : EJHG|June 2, 2021
A MT-TL1 variant identified by whole exome sequencing in an individual with intellectual disability, epilepsy, and spastic tetraparesisElke de Boer, Charlotte W Ockeloen, Leslie Matalonga, et al.Journal of Clinical Medicine|April 27, 2024
Infectious Diseases and Basal Ganglia Calcifications: A Cross-Sectional Study in Patients with Fahr's Disease and Systematic ReviewBirgitta M G Snijders, Mike J L Peters, Susanne van den Brink, et al.Scientific Reports|September 1, 2022
Ascorbate content of clinical glioma tissues is related to tumour grade and to global levels of 5-hydroxymethyl cytosineRebekah L I Crake, Eleanor R Burgess, George A R Wiggins, et al.American Journal of Human Genetics|December 14, 2011
Disruption of teashirt zinc finger homeobox 1 is associated with congenital aural atresia in humansIlse Feenstra, Lisenka E L M Vissers, Ronald J E Pennings, et al.European Journal of Human Genetics : EJHG|July 12, 2020
Overrepresentation of genetic variation in the AnkyrinG interactome is related to a range of neurodevelopmental disordersIlse M van der Werf, Sandra Jansen, Petra F de Vries, et al.American Journal of Preventive Cardiology|July 6, 2026
Impact of risk factor burden and vascular bed involvement on dementia risk in individuals with established cardiovascular diseaseJan F de Leijer, Geert Jan Biessels, Frank L J Visseren, et al.European Journal of Human Genetics : EJHG|October 26, 2021
Lessons learned from unsolicited findings in clinical exome sequencing of 16,482 individualsVyne van der Schoot, Lonneke Haer-Wigman, Ilse Feenstra, et al.Genome Medicine|May 9, 2023
Comprehensive de novo mutation discovery with HiFi long-read sequencingErdi Kucuk, Bart P G H van der Sanden, Luke O'Gorman, et al.Pageof 41