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Journal of Thrombosis and Haemostasis : JTH|April 26, 2006
Genetic linkage and association analysis in type 1 von Willebrand disease: results from the Canadian type 1 VWD studyP D James, A D Paterson, C Notley, et al.
Journal of Medical Genetics|September 1, 1994
Study of the Huntington's disease (HD) gene CAG repeats in schizophrenic patients shows overlap of the normal and HD affected ranges but absence of correlation with schizophreniaD C Rubinsztein, J Leggo, S Goodburn, et al.
Nature Genetics|July 1, 1995
Microsatellite evolution--evidence for directionality and variation in rate between speciesD C Rubinsztein, W Amos, J Leggo, et al.
Nature Genetics|August 1, 1994
Mutational bias provides a model for the evolution of Huntington's disease and predicts a general increase in disease prevalenceD C Rubinsztein, W Amos, J Leggo, et al.
American Journal of Medical Genetics|April 9, 1996
Analysis of thirteen trinucleotide repeat loci as candidate genes for schizophrenia and bipolar affective disorderS Jain, J Leggo, L E DeLisi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 1, 1997
Dentatorubral and pallidoluysian atrophy (DRPLA). Clinical and neuropathological findings in genetically confirmed North American and European pedigreesM W Becher, D C Rubinsztein, J Leggo, et al.
Neurology|July 23, 1998
Patients with features similar to Huntington's disease, without CAG expansion in huntingtinA Rosenblatt, N G Ranen, D C Rubinsztein, et al.
American Journal of Human Genetics|July 1, 1996
Phenotypic characterization of individuals with 30-40 CAG repeats in the Huntington disease (HD) gene reveals HD cases with 36 repeats and apparently normal elderly individuals with 36-39 repeatsD C Rubinsztein, J Leggo, R Coles, et al.
Human Molecular Genetics|May 1, 1996
cDNA cloning of a human homologue of the Caenorhabditis elegans cell fate-determining gene mab-21: expression, chromosomal localization and analysis of a highly polymorphic (CAG)n trinucleotide repeatR L Margolis, O C Stine, M G McInnis, et al.
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