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Molecular Syndromology|October 27, 2016
Generalized Epilepsy and Myoclonic Seizures in 22q11.2 Deletion SyndromeVincent Strehlow, Marielle E M Swinkels, Rhys H Thomas, et al.
Neurology. Genetics|July 14, 2017
Loss-of-function variants of <i>SCN8A</i> in intellectual disability without seizuresJacy L Wagnon, Bryan S Barker, Matteo Ottolini, et al.
European Journal of Human Genetics : EJHG|November 28, 2013
Structural genomic variation in childhood epilepsies with complex phenotypesIngo Helbig, Marielle E M Swinkels, Emmelien Aten, et al.
Brain : a Journal of Neurology|October 22, 2009
Recurrent microdeletions at 15q11.2 and 16p13.11 predispose to idiopathic generalized epilepsiesCarolien G F de Kovel, Holger Trucks, Ingo Helbig, et al.
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