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The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|August 23, 2011
Founder mutation for α-sarcoglycan-LGMD2D in a Magdalen Islands Acadian clusterM Tétreault, M Srour, J Allyson, et al.Neurology|November 14, 2007
A novel founder SCN4A mutation causes painful cold-induced myotonia in French-CanadiansE Rossignol, J Mathieu, I Thiffault, et al.Brain : a Journal of Neurology|September 30, 2006
A novel autosomal recessive limb-girdle muscular dystrophy with quadriceps atrophy maps to 11p13-p12J Jarry, M F Rioux, V Bolduc, et al.Brain : a Journal of Neurology|June 9, 2006
A new form of congenital muscular dystrophy with joint hyperlaxity maps to 3p23-21M Tétreault, A Duquette, I Thiffault, et al.Clinical Genetics|September 1, 2017
Recessive mutations in NDUFA2 cause mitochondrial leukoencephalopathyS Perrier, L Gauquelin, M Tétreault, et al.NPJ Genomic Medicine|August 12, 2025
Rapid generation of a sdhb loss-of-function zebrafish model for secreting pheochromocytomas and paragangliomasS Parisien-La Salle, F Nobilleau, A da Silva Babinet, et al.Clinical Genetics|July 22, 2014
Whole-exome sequencing broadens the phenotypic spectrum of rare pediatric epilepsy: a retrospective studyD A Dyment, M Tétreault, C L Beaulieu, et al.Clinical Genetics|July 15, 2017
Whole-exome sequencing is a valuable diagnostic tool for inherited peripheral neuropathies: Outcomes from a cohort of 50 familiesT Hartley, J D Wagner, J Warman-Chardon, et al.Clinical Genetics|February 8, 2017
Debunking Occam's razor: Diagnosing multiple genetic diseases in families by whole-exome sequencingT B Balci, T Hartley, Y Xi, et al.Pageof 1