An autosomal dominant disorder with episodic ataxia, vertigo, and tinnitus. by Steckley, J, Ebers, G, Cader, M, McLachlan, R

A genome-wide screen and linkage mapping for a large pedigree with episodic ataxia. by Cader, M, Steckley, J, Dyment, D, McLachlan, R, Ebers, G

Genetic analysis of vitamin D pathway genes in multiple sclerosis by Steckley, J, Dyment, D, Sadovnick, D, Risch, N, Ebers, G, Grp, C

Genetic analysis of vitamin D related genes in Canadian multiple sclerosis patients. Canadian Collaborative Study Group. by Steckley, J, Dyment, D, Sadovnick, A, Risch, N, Hayes, C, Ebers, G

CCR5 does not influence genetic susceptibility to multiple sclerosis in the Canadian population. by Steckley, J, Cousin, K, Sadovnick, A, Risch, N, Ebers, G, Grp, C

Genetic analysis of vitamin D related genes in Canadian multiple sclerosis patients by Steckley, J, Dyment, D, Sadovnick, A, Risch, N, Hayes, C, Ebers, G, Grp, C

No evidence to support CTLA-4 as a susceptibility gene in MS families: the Canadian Collaborative Study. by Dyment, D, Steckley, J, Willer, C, Armstrong, H, Sadovnick, A, Risch, N, Ebers, G

A genome-wide scan for regions shared identical by descent in Hutterite MS families by Dyment, D, Datta, A, Steckley, J, Willer, C, Sadovnick, A, Risch, N, Hader, W, Ebers, G

TCR beta polymorphisms and multiple sclerosis. by Dyment, D, Steckley, J, Morrison, K, Willer, C, Cader, M, DeLuca, G, Sadovnick, A, Risch, N, Ebers, G