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Characterization of a novel SPG3A deletion in a french-canadian familyMEIJER, Inge A; DION, Patrick; SODERBLOM, Cynthia et al.Annals of neurology. 2007, Vol 61, Num 6, pp 599-603, issn 0364-5134, 5 p.Article

Diversity of ARSACS Mutations in French-CanadiansTHIFFAULT, I; DICAIRE, M. J; MCPHERSON, P. S et al.Canadian journal of neurological sciences. 2013, Vol 40, Num 1, pp 61-66, issn 0317-1671, 6 p.Article

Adrenomyeloneuropathy : Report of a new mutation in a French Canadian femaleDIONNE, Annie; BRUNET, Denis; MCCAMPBELL, Alexander et al.Canadian journal of neurological sciences. 2005, Vol 32, Num 2, pp 261-263, issn 0317-1671, 3 p.Article

A fille du roy introduced the T14484C leber hereditary optic neuropathy mutation in French CanadiansLABERGE, Anne-Marie; JOMPHE, Michèle; BRAIS, Bernard et al.American journal of human genetics. 2005, Vol 77, Num 2, pp 313-317, issn 0002-9297, 5 p.Article

Cladistic analysis of the apolipoprotein AI-CIII-AIV gene cluster using a healthy French Canadian sample. I: Haploid analysisHAVILAND, M. B; KESSLING, A. M; DAVIGNON, J et al.Annals of human genetics. 1995, Vol 59, pp 211-231, issn 0003-4800, 2Article

Résultats préliminaires d'une enquête sur les habitudes alimentaires des canadiens français à Montréal = Food habits of french canadians in Montreal, QuebecPARVIZ GHADIRIAN, P; THOUEZ, J.-P.Médecine et nutrition. 1996, Vol 32, Num 1, pp 28-37, issn 0398-7604Article

Variability of the genetic contribution of Quebec population founders associated to some deleterious genesHEYER, E; TREMBLAY, M.American journal of human genetics. 1995, Vol 56, Num 4, pp 970-978, issn 0002-9297Article

The 14q restless legs syndrome locus in the French Canadian populationLEVCHENKO, Anastasia; MONTPLAISIR, Jacques-Yves; ROULEAU, Guy A et al.Annals of neurology. 2004, Vol 55, Num 6, pp 887-891, issn 0364-5134, 5 p.Article

Variations sur l'impact des processus démographiques sur la diversité génétique = Variations on the impact of demographic processes on genetic diversityAusterlitz, Frédéric; Gouyon, Pierre-Henri.1999, 182 p.Thesis

Mitochondrial DNA polymorphism detected with the restriction enzymes BstNI and BclI in a French Canadian populationGELINAS, Y; TURCOTTE, L; BOUCHARD, C et al.Annals of human genetics. 1989, Vol 53, Num 4, pp 319-325, issn 0003-4800Article

Hereditary ataxia, spastic paraparesis and neuropathy in the French-Canadian populationDUPRE, Nicolas; BOUCHARD, Jean-Pierre; BRAIS, Bernard et al.Canadian journal of neurological sciences. 2006, Vol 33, Num 2, pp 149-157, issn 0317-1671, 9 p.Article

Quantitative founder-effect analysis of french canadian families identifies specific loci contributing to metabolic phenotypes of hypertensionHARRIET, P; MERLO, E; ANTONIOL, G et al.American journal of human genetics. 2005, Vol 76, Num 5, pp 815-832, issn 0002-9297, 18 p.Article

Mycobacterium ulcerans infection (Buruli ulcer) : First reported case in a travelerSEMRET, M; KOROMIHIS, G; MACLEAN, J. D et al.The American journal of tropical medicine and hygiene. 1999, Vol 61, Num 5, pp 689-693, issn 0002-9637Article

Reproductive life of French-Canadians in the 17-18th centuries : a search for a trade-off between early fecundity and longevityLE BOURG, E; THON, B; LEGARE, J et al.Experimental gerontology. 1993, Vol 28, Num 3, pp 217-232, issn 0531-5565Article

Founder effect in familial hyperchylomicronemia among French Canadians of QuebecDE BRAEKELEER, M; DIONNE, C; GAGNE, C et al.Human heredity. 1991, Vol 41, Num 3, pp 168-173, issn 0001-5652Article

Hereditary disorders in Saguenay-Lac-St-Jean (Quebec, Canada)DE BRAEKELEER, M.Human heredity. 1991, Vol 41, Num 3, pp 141-146, issn 0001-5652Article

A novel founder SCN4A mutation causes painful cold-induced myotonia in French-CanadiansROSSIGNOL, E; MATHIEU, J; THIFFAULT, I et al.Neurology. 2007, Vol 69, Num 20, pp 1937-1941, issn 0028-3878, 5 p.Article

Les archives des francophones de la louisiane = Francophone archives of LouisianaCLIFTON, Deborah J; HARDY, Florent; TURNER, Bruce et al.Archives (Québec). 2004, Vol 36, Num 2, pp 23-37, issn 0044-9423, 15 p.Article

Bone mineral density in French Canadian womenBLANCHET, C; DODIN, S; DUMONT, M et al.Osteoporosis international. 1998, Vol 8, Num 3, pp 268-273, issn 0937-941XArticle

Assessment of French patients with LPL deficiency for French Canadian mutationsFOUBERT, L; DE GENNES, J. L; LAGARDE, J. P et al.Journal of medical genetics. 1997, Vol 34, Num 8, pp 672-675, issn 0022-2593Article

Description and analysis of allele distribution for four VNTR markers in French and French Canadian populationsMONSON, K. L; MOISAN, J.-P; PASCAL, O et al.Human heredity. 1995, Vol 45, Num 3, pp 135-143, issn 0001-5652Article

Impact of a common mutation of the LDL receptor gene, in French-Canadian patients with familial hypercholesterolemia, on means, variances and correlations among traits of lipid metabolismROY, M; SING, C. F; BETARD, C et al.Clinical genetics. 1995, Vol 47, Num 2, pp 59-67, issn 0009-9163Article

Genetic epidemiology of cystic fibrosis in Saguenay-Lac-St-Jean (Quebec, Canada)DAIGNEAULT, J; AUBIN, G; SIMARD, F et al.Clinical genetics. 1991, Vol 40, Num 4, pp 298-303, issn 0009-9163Article

Mutations in C5ORF42 Cause Joubert Syndrome in the French Canadian PopulationSROUR, Myriam; SCHWARTZENTRUBER, Jeremy; BOYCOTT, Kym M et al.American journal of human genetics. 2012, Vol 90, Num 4, pp 693-700, issn 0002-9297, 8 p.Article