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American Journal of Human Genetics|April 10, 2002
Krit1 missense mutations lead to splicing errors in cerebral cavernous malformationDominique J Verlaan, Adrian M Siegel, Guy A RouleauHuman Mutation|December 24, 2008
The proportion of mutations predicted to have a deleterious effect differs between gain and loss of function genes in neurodegenerative diseasePaul N Valdmanis, Dominique J Verlaan, Guy A RouleauGenome Research|July 17, 2009
A probabilistic approach for SNP discovery in high-throughput human resequencing dataRose Hoberman, Joana Dias, Bing Ge, et al.Annals of Neurology|September 30, 2004
A mutation in the HSN2 gene causes sensory neuropathy type II in a Lebanese familyJean-Baptiste Rivière, Dominique J Verlaan, Masoud Shekarabi, et al.Human Genetics|January 25, 2012
Interaction between genetic and epigenetic variation defines gene expression patterns at the asthma-associated locus 17q12-q21 in lymphoblastoid cell linesSoizik Berlivet, Sanny Moussette, Manon Ouimet, et al.Genome Biology|March 23, 2011
Genome-wide assessment of imprinted expression in human cellsLisanne Morcos, Bing Ge, Vonda Koka, et al.Journal of Immunology (Baltimore, Md. : 1950)|October 2, 2009
A cis-acting regulatory variant in the IL2RA locusHui-Qi Qu, Dominique J Verlaan, Bing Ge, et al.The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|May 31, 2003
Linkage to the CCM2 locus and genetic heterogeneity in familial cerebral cavernous malformationNicolas Dupré, Dominique J Verlaan, Collette K Hand, et al.Archives of Neurology|November 13, 2008
A novel duplication confirms the involvement of 5q23.2 in autosomal dominant leukodystrophyInge A Meijer, Ana A Simoes-Lopes, Sandra Laurent, et al.Annals of Neurology|June 3, 2004
The 14q restless legs syndrome locus in the French Canadian populationAnastasia Levchenko, Jacques-Yves Montplaisir, Marie-Pierre Dubé, et al.Pageof 2