Showing results (511-520 of 525) with videos related to
Sort By:
Pageof 53
Human Mutation|September 27, 2016
WRN Mutation Update: Mutation Spectrum, Patient Registries, and Translational ProspectsKoutaro Yokote, Sirisak Chanprasert, Lin Lee, et al.Journal of Neural Engineering|February 24, 2021
The Argo: a high channel count recording system for neural recording in vivoKunal Sahasrabuddhe, Aamir A Khan, Aditya P Singh, et al.Journal of Medical Genetics|March 11, 2020
Pathogenic variants in TNRC6B cause a genetic disorder characterised by developmental delay/intellectual disability and a spectrum of neurobehavioural phenotypes including autism and ADHDJorge Luis Granadillo, Alexander P A Stegmann, Hui Guo, et al.Physical Review Letters|October 15, 2008
Limits on spin-dependent WIMP-nucleon cross sections from the XENON10 experimentJ Angle, E Aprile, F Arneodo, et al.Physical Review Letters|August 27, 2011
Search for light dark matter in XENON10 dataJ Angle, E Aprile, F Arneodo, et al.Physical Review Letters|February 1, 2008
First results from the XENON10 dark matter experiment at the Gran Sasso National LaboratoryJ Angle, E Aprile, F Arneodo, et al.Journal of the American College of Radiology : JACR|February 6, 2026
Recommendations From the Blue Ribbon Panel on Fluoroscopy SafetyDustin A Gress, M Mahesh, Kevin W Dickey, et al.The New England Journal of Medicine|September 14, 2012
Phenotypic heterogeneity of genomic disorders and rare copy-number variantsSanthosh Girirajan, Jill A Rosenfeld, Bradley P Coe, et al.Journal of the American Society of Nephrology : JASN|August 23, 2014
Urinary tract effects of HPSE2 mutationsHelen M Stuart, Neil A Roberts, Emma N Hilton, et al.European Journal of Human Genetics : EJHG|November 27, 2014
Further delineation of the KAT6B molecular and phenotypic spectrumTamsin Gannon, Rahat Perveen, Hélene Schlecht, et al.Pageof 53