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Human Genetics
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May 1, 1991
Localisation of the myotonic dystrophy locus to 19q13.2-19q13.3 and its relationship to twelve polymorphic loci on 19q
H 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 mutation
J 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 dystrophy
C 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 marker
H 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 stroke
R 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 disease
E 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 horses
K 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 19q
G 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 19
D 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 dystrophy
H G Harley, S A Rundle, J C MacMillan, et al.
Page
of 19
Search research articles
Search
Showing results (161-170 of 187) with videos related to
Sort By:
Page
of 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 19q
H 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 mutation
J 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 dystrophy
C 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 marker
H 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 stroke
R 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 disease
E 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 horses
K 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 19q
G 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 19
D 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 dystrophy
H G Harley, S A Rundle, J C MacMillan, et al.
Page
of 19