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Clinical Genetics|August 1, 2014
Germline BAP1 mutations predispose also to multiple basal cell carcinomasA de la Fouchardière, O Cabaret, L Savin, et al.The Journal of Hospital Infection|February 10, 2009
Decontamination of prion protein (BSE301V) using a genetically engineered proteaseJ Dickinson, H Murdoch, M J Dennis, et al.American Journal of Medical Genetics|December 5, 2000
Clinical variability and genetic homogeneity of the camptodactyly-arthropathy-coxa vara-pericarditis syndromeL Faivre, A M Prieur, M Le Merrer, et al.Human Molecular Genetics|September 16, 1998
Segregation of a missense mutation in the microtubule-associated protein tau gene with familial frontotemporal dementia and parkinsonismC Dumanchin, A Camuzat, D Campion, et al.Annals of Neurology|April 1, 1996
Spinocerebellar ataxia 3 and Machado-Joseph disease: clinical, molecular, and neuropathological featuresA Dürr, G Stevanin, G Cancel, et al.Journal of Medical Genetics|August 1, 1996
No founder effect in three novel Alzheimer's disease families with APP 717 Val-->Ile mutation. Clerget-darpoux. French Alzheimer's Disease Study GroupD Campion, A Brice, D Hannequin, et al.European Journal of Human Genetics : EJHG|August 22, 2000
Linkage disequilibrium in inbred North African families allows fine genetic and physical mapping of triple A syndromeS Hadj-Rabia, R Salomon, A Pelet, et al.European Journal of Human Genetics : EJHG|September 12, 2000
APOE promoter polymorphisms do not confer independent risk for Alzheimer's disease in a French populationL Zurutuza, P Verpillat, G Raux, et al.Neurology|February 28, 2007
Variations in the APP gene promoter region and risk of Alzheimer diseaseL Guyant-Maréchal, A Rovelet-Lecrux, L Goumidi, et al.Human Molecular Genetics|April 10, 1999
Genome-wide scan for autism susceptibility genes. Paris Autism Research International Sibpair StudyA Philippe, M Martinez, M Guilloud-Bataille, et al.Pageof 4