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Iscience|May 10, 2021
Comparative analysis of antibodies to SARS-CoV-2 between asymptomatic and convalescent patientsConnor J Dwyer, Colleen A Cloud, Cindy Wang, et al.Human Genetics|August 10, 2006
Clinical and molecular genetic features of ARC syndromePaul Gissen, Louise Tee, Colin A Johnson, et al.Journal of Medical Genetics|August 10, 2014
The clinical significance of small copy number variants in neurodevelopmental disordersReza Asadollahi, Beatrice Oneda, Pascal Joset, et al.Nature Methods|March 2, 2019
Author Correction: Stability, affinity, and chromatic variants of the glutamate sensor iGluSnFRJonathan S Marvin, Benjamin Scholl, Daniel E Wilson, et al.Epilepsia|February 7, 2017
Heterozygous truncation mutations of the SMC1A gene cause a severe early onset epilepsy with cluster seizures in females: Detailed phenotyping of 10 new casesJoseph D Symonds, Shelagh Joss, Kay A Metcalfe, et al.Nature Methods|January 4, 2019
Publisher Correction: Stability, affinity, and chromatic variants of the glutamate sensor iGluSnFRJonathan S Marvin, Benjamin Scholl, Daniel E Wilson, et al.Nature Methods|November 1, 2018
Stability, affinity, and chromatic variants of the glutamate sensor iGluSnFRJonathan S Marvin, Benjamin Scholl, Daniel E Wilson, et al.Brain : a Journal of Neurology|February 9, 2022
Activating RAC1 variants in the switch II region cause a developmental syndrome and alter neuronal morphologySiddharth Banka, Abigail Bennington, Martin J Baker, et al.American Journal of Medical Genetics. Part A|September 27, 2016
Clinical and genetic aspects of KBG syndromeKaren Low, Tazeen Ashraf, Natalie Canham, et al.Nature Ecology & Evolution|November 1, 2017
Genome expansion and lineage-specific genetic innovations in the forest pathogenic fungi ArmillariaGyörgy Sipos, Arun N Prasanna, Mathias C Walter, et al.Pageof 20