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Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 17, 2012
[Diagnostic investigations for an unexplained developmental disability]A Verloes, D Héron, T Billette de Villemeur, et al.Journal of Medical Genetics|July 7, 2009
Novel FOXG1 mutations associated with the congenital variant of Rett syndromeM A Mencarelli, A Spanhol-Rosseto, R Artuso, et al.Journal of Medical Genetics|August 30, 2008
Refinement of cortical dysgeneses spectrum associated with TUBA1A mutationsN Bahi-Buisson, K Poirier, N Boddaert, et al.Molecular Genetics and Metabolism|June 12, 2013
Renal transplantation in 4 patients with methylmalonic aciduria: a cell therapy for metabolic diseaseA Brassier, O Boyer, V Valayannopoulos, et al.Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|March 27, 2021
Electro-clinical features in epileptic children with chromosome 15q duplication syndromeM-T Dangles, V Malan, G Dumas, et al.Neurology|March 26, 2008
Myoclonus-dystonia: clinical and electrophysiologic pattern related to SGCE mutationsE Roze, E Apartis, F Clot, et al.Journal of Medical Genetics|June 5, 2010
Microdeletion at chromosome 4q21 defines a new emerging syndrome with marked growth restriction, mental retardation and absent or severely delayed speechC Bonnet, J Andrieux, M Béri-Dexheimer, et al.Pageof 5