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European Journal of Human Genetics : EJHG|January 22, 2009
IFIH1-GCA-KCNH7 locus is not associated with genetic susceptibility to multiple sclerosis in French patientsNicolas Couturier, Pierre-Antoine Gourraud, Isabelle Cournu-Rebeix, et al.Human Genetics|July 3, 2007
A novel locus for autosomal dominant "uncomplicated" hereditary spastic paraplegia maps to chromosome 8p21.1-q13.3Sylvain Hanein, Alexandra Dürr, Pascale Ribai, et al.European Journal of Human Genetics : EJHG|October 23, 2003
Meta and pooled analysis of European coeliac disease dataMarie-Claude Babron, Staffan Nilsson, Svetlana Adamovic, et al.Plos One|February 7, 2015
Homozygous STIL mutation causes holoprosencephaly and microcephaly in two siblingsCharlotte Mouden, Marie de Tayrac, Christèle Dubourg, et al.Journal of Neuroimmunology|October 25, 2003
Genetic analysis of multiple sclerosis in Europeans: French dataMehdi Alizadeh, Emmanuelle Génin, Marie-Claude Babron, et al.Carcinogenesis|March 3, 2012
Lung cancer and DNA repair genes: multilevel association analysis from the International Lung Cancer ConsortiumRémi Kazma, Marie-Claude Babron, Valérie Gaborieau, et al.Annals of Neurology|July 3, 2003
Genetic interaction of CTLA-4 with HLA-DR15 in multiple sclerosis patientsMehdi Alizadeh, Marie-Claude Babron, Brigitte Birebent, et al.Neurogenetics|November 5, 2003
Investigation of seven proposed regions of linkage in multiple sclerosis: an American and French collaborative studyMargaret A Pericak-Vance, Jackie B Rimmler, Jonathan L Haines, et al.Genetic Epidemiology|November 30, 2007
Linkage analyses of rheumatoid arthritis and related quantitative phenotypes: the GAW15 experienceSaurabh Ghosh, Marie-Claude Babron, Christopher I Amos, et al.American Journal of Human Genetics|June 15, 2007
Pleiotropic effects of CEP290 (NPHP6) mutations extend to Meckel syndromeLekbir Baala, Sophie Audollent, Jéléna Martinovic, et al.Pageof 4