The mutational spectrum of type 1 von Willebrand disease: results from a Canadian cohort study von James, Paula D., Notley, Colleen, Hegadorn, Carol, Leggo, Jayne, Tuttle, Angie, Tinlin, Shawn, Brown, Christine, Andrews, Chandler, Labelle, Andrea, Chirinian, Yvette, O'Brien, Lee, Othman, Maha, Rivard, Georges, Rapson, Dilys, Hough, Christine, Lillicrap, David

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The Canadian “National Program for hemophilia mutation testing” database: A ten‐year review von Natalia, Rydz, Jayne, Leggo, Shawn, Tinlin, Paula, James, David, Lillicrap

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Genotypes at the GluR6 Kainate Receptor Locus are Associated with Variation in the Age of Onset of Huntington Disease von Rubinsztein, David C., Leggo, Jayne, Chiano, Mathias, Dodge, Alan, Norbury, Gail, Rosser, Elisabeth, Craufurd, David

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Frequency of Platelet type versus Type 2B von Willebrand Disease von Hamilton, Alexander, Ozelo, Margareth, Leggo, Jayne, Notley, Colleen, Brown, Hannah, Pablo Frontroth, Juan, Angelillo-Scherrer, Anne, Baghaei, Fariba, Enayat, Said M., Favaloro, Emmanuel, Lillicrap, David, Othman, Maha

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The mutational spectrum of type 1 von Willebrand disease: results from a Canadian cohort study von James, P. D., Notley, C., Hegadorn, C., Leggo, J., Tuttle, A., Tinlin, S., Brown, C., Andrews, C., Labelle, A., Chirinian, Y., O'Brien, L., Othman, M., Rivard, G., Rapson, D., Hough, C., Lillicrap, D.

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Mutational bias provides a model for the evolution of Huntington's disease and predicts a general increase in disease prevalence von Rubinsztein, David C, Amos, William, Leggo, Jayne, Goodburn, Sandy, Ramesar, Rajkumar S, Old, John, Bontrop, Ronald, McMahon, Robert, Barton, David E, Ferguson-Smith, Malcolm A

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The Canadian “National Program for hemophilia mutation testing” database: A ten‐year review

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Frequency of Platelet type versus Type 2B von Willebrand Disease: An international registry-based study von HAMILTON, Alexander, OZELO, Margareth, LILLICRAP, David, OTHMAN, Maha, LEGGO, Jayne, NOTLEY, Colleen, BROWN, Hannah, FRONTROTH, Juan Pablo, ANGELILLO-SCHERRER, Anne, BAGHAEI, Fariba, ENAYAT, Said M, FAVALORO, Emmanuel

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Clearance and Genetic Variability of Von Willebrand Factor Are Major Determinants of the Pharmacokinetic Behavior of Factor VIII Concentrates in the Treatment of Pediatric Hemophil... von Ogiwara, Kenichi, Swystun, Laura L, Georgescu, Ilinca, Brown, Christine, Tuttle, Angie, Tinlin, Shawn, Leggo, Jayne, Albánez, Silvia, Carcao, Manuel, Blanchette, Victor S., Male, Christoph, Thom, Katharina, Lillicrap, David

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Aminoglycoside suppression of nonsense mutations in severe hemophilia von James, Paula D., Raut, Sanj, Rivard, Georges E., Poon, Man-Chiu, Warner, Margaret, McKenna, Susan, Leggo, Jayne, Lillicrap, David

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Haplotype analysis of the Δ2642 and (CAG)n polymorphisms in the Huntington's disease (HD) gene provides an explanation for an apparent ‘founder’ HD haplotype von Rubinsztein, David C., Leggo, Jayne, Goodburn, Sandy, Barton, David E., Ferguson-Smith, Malcolm A.

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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 wit... von Rubinsztein, D C, Leggo, J, Coles, R, Almqvist, E, Biancalana, V, Cassiman, J J, Chotai, K, Connarty, M, Crauford, D, Curtis, A, Curtis, D, Davidson, M J, Differ, A M, Dode, C, Dodge, A, Frontali, M, Ranen, N G, Stine, O C, Sherr, M, Abbott, M H, Franz, M L, Graham, C A, Harper, P S, Hedreen, J C, Hayden, M R

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Microsatellite evolution - evidence for directionality and variation in rate between species von Goodburn, Sandy, Margolis, Russell L, Amos, William, Jain, Sanjeev, Li, Shi-Hua, Leggo, Jayne, Ross, Christopher A, Rubinsztein, David C, Ferguson-Smith, Malcolm A

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Analysis of spinocerebellar ataxia types 1, 2, 3, and 6, dentatorubral-pallidoluysian atrophy, and Friedreich's ataxia genes in spinocerebellar ataxia patients in the UK von Leggo, J, Dalton, A, Morrison, P J, Dodge, A, Connarty, M, Kotze, M J, Rubinsztein, D C

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The mutational spectrum of type 1 von Willebrand disease : results from a Canadian cohort study. Commentary von SADLER, J. Evan, JAMES, Paula D, CHIRINIAN, Yvette, O'BRIEN, Lee, OTHMAN, Maha, RIVARD, Georges, RAPSON, Dilys, HOUGH, Christine, LILLICRAP, David, NOTLEY, Colleen, HEGADORN, Carol, LEGGO, Jayne, TUTTLE, Angie, TINLIN, Shawn, BROWN, Christine, ANDREWS, Chandler, LABELLE, Andrea

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Microsatellites evolve more rapidly in humans than in chimpanzees von RUBINSZTEIN, D. C, LEGGO, J, AMOS, W

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Non-Mendelian transmission at the Machado-Joseph disease locus in normal females: preferential transmission of alleles with smaller CAG repeats von Rubinsztein, D C, Leggo, J

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Sequence variation and size ranges of CAG repeats in the Machado-Joseph disease, spinocerebellar ataxia type 1 and androgen receptor genes von Rubinsztein, David C., Leggo, Jayne, Coetzee, Gerhard A., Irvine, Ryan A., Buckley, Michael, Ferguson-Smith, Malcolm A.

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Analysis of the 5' upstream sequence of the Huntington's disease (HD) gene shows six new rare alleles which are unrelated to the age at onset of HD von Coles, R, Leggo, J, Rubinsztein, D C

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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... von Margolis, Russell L., Colin Stine, O., McInnis, Melvin G., Ranen, Neal G., Rubinsztein, David C., Leggo, Jayne, Jones Brando, Lorraine V., Kidwai, Arif S., Loev, Scott J., Breschel, Theresa S., Callahan, Colleen, Simpson, Sylvia G., Raymond DePaulo, J., McMahon, Francis J., Jain, Sanjeev, Paykel, Eugene S., Walsh, Cathy, DeLisi, Lynn E., Crow, Timothy J., Fuller Torrey, E., Ashworth, Roxann G., Macke, Jennifer P., Nathans, Jeremy, Ross, Christopher A.

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