Showing results (11-20 of 25) with videos related to
Sort By:
Pageof 3
American Journal of Medical Genetics|July 15, 1994
Male with typical fragile X phenotype is deleted for part of the FMR1 gene and for about 100 kb of upstream regionY Trottier, G Imbert, A Poustka, et al.Neurorx : the Journal of the American Society for Experimental Neurotherapeutics|February 21, 2006
Central nervous system drug development: an integrative biomarker approach toward individualized medicineB Gomez-Mancilla, E Marrer, J Kehren, et al.Clinical Microbiology and Infection : the Official Publication of the European Society of Clinical Microbiology and Infectious Diseases|April 3, 2004
Causative organisms of infective endocarditis according to host statusK Barrau, A Boulamery, G Imbert, et al.Nature|November 23, 1995
Polyglutamine expansion as a pathological epitope in Huntington's disease and four dominant cerebellar ataxiasY Trottier, Y Lutz, G Stevanin, et al.Infection|June 3, 2008
Bacillus licheniformis septicemia in a very-low-birth-weight neonate: a case reportA Lépine, F Michel, C Nicaise, et al.Nature Genetics|May 1, 1995
Cellular localization of the Huntington's disease protein and discrimination of the normal and mutated formY Trottier, D Devys, G Imbert, et al.La Revue De Medecine Interne|November 14, 2008
[Liver disease and pregnancy]C Delluc, N Costedoat-Chalumeau, G Leroux, et al.Journal of Clinical Microbiology|October 7, 2005
Contribution of systematic serological testing in diagnosis of infective endocarditisD Raoult, J P Casalta, H Richet, et al.Annals of Neurology|December 10, 1997
Differential distribution of the normal and mutated forms of huntingtin in the human brainI Gourfinkel-An, G Cancel, Y Trottier, et al.Nature Genetics|November 1, 1996
Cloning of the gene for spinocerebellar ataxia 2 reveals a locus with high sensitivity to expanded CAG/glutamine repeatsG Imbert, F Saudou, G Yvert, et al.Pageof 3