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Proceedings of the National Academy of Sciences of the United States of America|April 15, 1997
Genotypes at the GluR6 kainate receptor locus are associated with variation in the age of onset of Huntington diseaseD C Rubinsztein, J Leggo, M Chiano, et al.Human Molecular Genetics|September 1, 1995
Sequence variation and size ranges of CAG repeats in the Machado-Joseph disease, spinocerebellar ataxia type 1 and androgen receptor genesD C Rubinsztein, J Leggo, G A Coetzee, et al.Neurology|September 26, 1997
Homozygotes and heterozygotes for ciliary neurotrophic factor null alleles do not show earlier onset of Huntington's diseaseD C Rubinsztein, J Leggo, M Chiano, et al.Journal of Medical Genetics|January 16, 1998
Analysis of spinocerebellar ataxia types 1, 2, 3, and 6, dentatorubral-pallidoluysian atrophy, and Friedreich's ataxia genes in spinocerebellar ataxia patients in the UKJ Leggo, A Dalton, P J Morrison, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|February 9, 2007
Different clinical phenotype in triplets with haemophilia AC Barnes, V Blanchette, D Lillicrap, et al.American Journal of Medical Genetics|September 20, 1996
Analysis of polyglutamine-coding repeats in the TATA-binding protein in different human populations and in patients with schizophrenia and bipolar affective disorderD C Rubinsztein, J Leggo, T J Crow, et al.Journal of Thrombosis and Haemostasis : JTH|July 23, 2003
Intensive exposure to factor VIII is a risk factor for inhibitor development in mild hemophilia AA Sharathkumar, D Lillicrap, V S Blanchette, et al.Annals of Human Genetics|June 21, 2001
Genetic diversity at the FMR1 locus in the Indonesian populationS M Faradz, M Z Pattiiha, D A Leigh, et al.Annals of Human Genetics|June 28, 2001
Distribution of FMR1 and FMR2 alleles in Javanese individuals with developmental disability and confirmation of a specific AGG-interruption pattern in Asian populationsS M Faradz, J Leggo, A Murray, et al.Journal of Thrombosis and Haemostasis : JTH|January 15, 2013
The genetics of Canadian type 3 von Willebrand disease: further evidence for co-dominant inheritance of mutant allelesM Bowman, A Tuttle, C Notley, et al.Pageof 3