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Molecular Psychiatry|October 26, 2011
Emerging major synaptic signaling pathways involved in intellectual disabilityA Pavlowsky, J Chelly, P BilluartCell|October 24, 2001
Regulating axon branch stability: the role of p190 RhoGAP in repressing a retraction signaling pathwayP Billuart, C G Winter, A Maresh, et al.Clinical Genetics|September 30, 2017
Autism spectrum disorder recurrence, resulting of germline mosaicism for a CHD2 gene missense variantN Lebrun, P Parent, J Gendras, et al.Neuroscience|September 6, 2015
Identification of intellectual disability genes showing circadian clock-dependent expression in the mouse hippocampusJ Renaud, F Dumont, M Khelfaoui, et al.Molecular and Cellular Neurosciences|October 10, 2001
Doublecortin interacts with mu subunits of clathrin adaptor complexes in the developing nervous systemG Friocourt, P Chafey, P Billuart, et al.Annales De Genetique|May 20, 2000
Determination of the gene structure of human oligophrenin-1 and identification of three novel polymorphisms by screening of DNA from 164 patients with non-specific X-linked mental retardationP Billuart, J Chelly, A Carrié, et al.American Journal of Human Genetics|April 1, 1997
A gene for dominant nonspecific X-linked mental retardation is located in Xq28V des Portes, P Billuart, A Carrié, et al.American Journal of Medical Genetics|October 23, 1997
Gene for nonspecific X-linked mental retardation (MRX 47) is located in Xq22.3-q24V des Portes, N Soufir, A Carrié, et al.Journal of Thrombosis and Haemostasis : JTH|January 6, 2015
Loss of oligophrenin1 leads to uncontrolled Rho activation and increased thrombus formation in miceA Fotinos, M Klier, N S Gowert, et al.Clinical Genetics|June 4, 1998
Inherited microdeletion in Xp21.3-22.1 involved in non-specific mental retardationV des Portes, A Carrié, P Billuart, et al.Pageof 3