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Molecular Psychiatry|October 26, 2011
Emerging major synaptic signaling pathways involved in intellectual disabilityA Pavlowsky, J Chelly, P BilluartMolecular 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.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.Human Molecular Genetics|September 2, 1999
Breakthroughs in molecular and cellular mechanisms underlying X-linked mental retardationJ ChellyProceedings of the National Academy of Sciences of the United States of America|July 22, 1998
Somatic mutations of the beta-catenin gene are frequent in mouse and human hepatocellular carcinomasA de La Coste, B Romagnolo, P Billuart, et al.Human Molecular Genetics|July 1, 1996
Identification by STS PCR screening of a microdeletion in Xp21.3-22.1 associated with non-specific mental retardationP Billuart, M C Vinet, V des Portes, et al.Neurology|October 14, 2005
Oligophrenin 1 mutations frequently cause X-linked mental retardation with cerebellar hypoplasiaG Zanni, Y Saillour, M Nagara, et al.Pageof 14