Showing results (1441-1450 of 1,502) with videos related to

Sort By:
Pageof 151
European Journal of Human Genetics : EJHG|November 27, 2014
Further delineation of the KBG syndrome phenotype caused by ANKRD11 aberrationsCharlotte W Ockeloen, Marjolein H Willemsen, Sonja de Munnik, et al.
Cancer Discovery|April 4, 2024
Next Directions in the Neuroscience of Cancers Arising outside the CNSMoran Amit, Corina Anastasaki, Robert Dantzer, et al.
Investigative Ophthalmology & Visual Science|August 27, 2024
Frequency and Genetic Spectrum of Inherited Retinal Dystrophies in a Large Dutch Pediatric Cohort: The RD5000 ConsortiumPam A T Heutinck, L Ingeborgh van den Born, Maikel Vermeer, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation|July 24, 2023
MYH7 p.(Arg1712Gln) is pathogenic founder variant causing hypertrophic cardiomyopathy with overall relatively delayed onsetLuisa Marsili, Freyja H M van Lint, Francesco Russo, et al.
Stroke|November 4, 2021
Risk, Clinical Course, and Outcome of Ischemic Stroke in Patients Hospitalized With COVID-19: A Multicenter Cohort StudyWouter M Sluis, Marijke Linschoten, Julie E Buijs, et al.
American Journal of Human Genetics|November 25, 2010
Targeted next-generation sequencing of a 12.5 Mb homozygous region reveals ANO10 mutations in patients with autosomal-recessive cerebellar ataxiaSascha Vermeer, Alexander Hoischen, Rowdy P P Meijer, et al.
Neurology|July 24, 2015
Effect of vaccinations on seizure risk and disease course in Dravet syndromeNienke E Verbeek, Nicoline A T van der Maas, Anja C M Sonsma, et al.
Pageof 151