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Physical Review Letters|October 26, 2005
New limit on the neutrinoless betabeta decay of 130TeC Arnaboldi, D R Artusa, F T Avignone, et al.American Journal of Human Genetics|January 26, 2016
Recurrent Muscle Weakness with Rhabdomyolysis, Metabolic Crises, and Cardiac Arrhythmia Due to Bi-allelic TANGO2 MutationsSeema R Lalani, Pengfei Liu, Jill A Rosenfeld, et al.American Journal of Human Genetics|June 3, 2017
YY1 Haploinsufficiency Causes an Intellectual Disability Syndrome Featuring Transcriptional and Chromatin DysfunctionMichele Gabriele, Anneke T Vulto-van Silfhout, Pierre-Luc Germain, et al.Physical Review Letters|May 21, 2005
First results from the CERN axion solar telescopeK Zioutas, S Andriamonje, V Arsov, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 15, 2019
De novo and inherited variants in ZNF292 underlie a neurodevelopmental disorder with features of autism spectrum disorderGhayda M Mirzaa, Jessica X Chong, Amélie Piton, et al.Scientific Data|August 30, 2017
FANTOM5 CAGE profiles of human and mouse samplesShuhei Noguchi, Takahiro Arakawa, Shiro Fukuda, et al.Nature|March 28, 2014
A promoter-level mammalian expression atlas, Alistair R R Forrest, Hideya Kawaji, et al.Pageof 42