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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.Nature Ecology & Evolution|February 11, 2018
Author Correction: Genome expansion and lineage-specific genetic innovations in the forest pathogenic fungi ArmillariaGyörgy Sipos, Arun N Prasanna, Mathias C Walter, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 22, 2022
Clustered variants in the 5' coding region of TRA2B cause a distinctive neurodevelopmental syndromeFrancis Ramond, Caroline Dalgliesh, Mona Grimmel, et al.Biorxiv : the Preprint Server for Biology|December 22, 2025
Signaling induced biophysical disruption of repressed chromatin domains drives immune cell fateAlexia Martínez de Paz, Christopher R Chin, Mythili Ketavarapu, et al.European Journal of Human Genetics : EJHG|April 16, 2009
BCOR analysis in patients with OFCD and Lenz microphthalmia syndromes, mental retardation with ocular anomalies, and cardiac laterality defectsEmma Hilton, Jennifer Johnston, Sandra Whalen, et al.Annals of Neurology|June 10, 2020
SCN3A-Related Neurodevelopmental Disorder: A Spectrum of Epilepsy and Brain MalformationTariq Zaman, Katherine L Helbig, Jérôme Clatot, et al.Nature Neuroscience|November 8, 2016
A viral strategy for targeting and manipulating interneurons across vertebrate speciesJordane Dimidschstein, Qian Chen, Robin Tremblay, et al.Nature Reviews. Neuroscience|February 7, 2013
New insights into the classification and nomenclature of cortical GABAergic interneuronsJavier DeFelipe, Pedro L López-Cruz, Ruth Benavides-Piccione, et al.American Journal of Medical Genetics. Part A|May 27, 2017
Phenotypes and genotypes in individuals with SMC1A variantsSylvia Huisman, Paul A Mulder, Egbert Redeker, et al.Pageof 15