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D J Shaw

Showing results (161-170 of 187) with videos related to

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Human Genetics|May 1, 1991
Localisation of the myotonic dystrophy locus to 19q13.2-19q13.3 and its relationship to twelve polymorphic loci on 19qH G Harley, K V Walsh, S Rundle, et al.
Lancet (London, England)|October 16, 1993
Molecular analysis and clinical correlations of the Huntington's disease mutationJ C MacMillan, R G Snell, A Tyler, et al.
Human Genetics|January 1, 1985
Genetic linkage relationships of seven DNA probes with Duchenne and Becker muscular dystrophyC S Brown, N S Thomas, M Sarfarazi, et al.
American Journal of Human Genetics|July 1, 1991
Detection of linkage disequilibrium between the myotonic dystrophy locus and a new polymorphic DNA markerH G Harley, J D Brook, J Floyd, et al.
Neurogenetics|May 17, 2001
Mapping and sequencing rat dishevelled-1: a candidate gene for cerebral ischaemic insult in a rat model of strokeR P De Lange, K Burr, J S Clark, et al.
The Journal of Small Animal Practice|April 3, 2018
Immunohistochemical differentiation of reactive from malignant mesothelium as a diagnostic aid in canine pericardial diseaseE Milne, Y Martinez Pereira, C Muir, et al.
Clinical and Experimental Allergy : Journal of the British Society for Allergy and Clinical Immunology|October 25, 2007
Organic dust exposure increases mast cell tryptase in bronchoalveolar lavage fluid and airway epithelium of heaves horsesK J Dacre, B C McGorum, D J Marlin, et al.
Genomics|July 1, 1992
Physical and genetic characterization of the distal segment of the myotonic dystrophy area on 19qG Jansen, P J de Jong, C Amemiya, et al.
Human Genetics|November 1, 1986
Regional localisations and linkage relationships of seven RFLPs and myotonic dystrophy on chromosome 19D J Shaw, A L Meredith, M Sarfarazi, et al.
American Journal of Human Genetics|June 1, 1993
Size of the unstable CTG repeat sequence in relation to phenotype and parental transmission in myotonic dystrophyH G Harley, S A Rundle, J C MacMillan, et al.
Pageof 19

Showing results (161-170 of 187) with videos related to

Sort By:
Pageof 19
Human Genetics|May 1, 1991
Localisation of the myotonic dystrophy locus to 19q13.2-19q13.3 and its relationship to twelve polymorphic loci on 19qH G Harley, K V Walsh, S Rundle, et al.
Lancet (London, England)|October 16, 1993
Molecular analysis and clinical correlations of the Huntington's disease mutationJ C MacMillan, R G Snell, A Tyler, et al.
Human Genetics|January 1, 1985
Genetic linkage relationships of seven DNA probes with Duchenne and Becker muscular dystrophyC S Brown, N S Thomas, M Sarfarazi, et al.
American Journal of Human Genetics|July 1, 1991
Detection of linkage disequilibrium between the myotonic dystrophy locus and a new polymorphic DNA markerH G Harley, J D Brook, J Floyd, et al.
Neurogenetics|May 17, 2001
Mapping and sequencing rat dishevelled-1: a candidate gene for cerebral ischaemic insult in a rat model of strokeR P De Lange, K Burr, J S Clark, et al.
The Journal of Small Animal Practice|April 3, 2018
Immunohistochemical differentiation of reactive from malignant mesothelium as a diagnostic aid in canine pericardial diseaseE Milne, Y Martinez Pereira, C Muir, et al.
Clinical and Experimental Allergy : Journal of the British Society for Allergy and Clinical Immunology|October 25, 2007
Organic dust exposure increases mast cell tryptase in bronchoalveolar lavage fluid and airway epithelium of heaves horsesK J Dacre, B C McGorum, D J Marlin, et al.
Genomics|July 1, 1992
Physical and genetic characterization of the distal segment of the myotonic dystrophy area on 19qG Jansen, P J de Jong, C Amemiya, et al.
Human Genetics|November 1, 1986
Regional localisations and linkage relationships of seven RFLPs and myotonic dystrophy on chromosome 19D J Shaw, A L Meredith, M Sarfarazi, et al.
American Journal of Human Genetics|June 1, 1993
Size of the unstable CTG repeat sequence in relation to phenotype and parental transmission in myotonic dystrophyH G Harley, S A Rundle, J C MacMillan, et al.
Pageof 19