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D E Barton

Showing results (11-20 of 65) with videos related to

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Genomics|October 1, 1989
Level of expression and chromosome mapping of the mouse cholecystokinin gene: implications for murine models of genetic obesityJ M Friedman, B S Schneider, D E Barton, et al.
Genomics|October 1, 1987
The myelin-associated glycoprotein gene: mapping to human chromosome 19 and mouse chromosome 7 and expression in quivering miceD E Barton, M Arquint, J Roder, et al.
Neurology|July 27, 2005
Fragile X-associated tremor/ataxia syndrome presenting in a woman after chemotherapyJ P O'Dwyer, C Clabby, J Crown, et al.
Nature Genetics|November 1, 1993
Site of (CCG) polymorphism in the HD geneD C Rubinsztein, J Leggo, D E Barton, et al.
Journal of Medical Genetics|October 1, 1994
Chimaerism shown by cytogenetics and DNA polymorphism analysisA J Green, D E Barton, P Jenks, et al.
Human Molecular Genetics|October 1, 1993
Analysis of the huntingtin gene reveals a trinucleotide-length polymorphism in the region of the gene that contains two CCG-rich stretches and a correlation between decreased age of onset of Huntington's disease and CAG repeat numberD C Rubinsztein, D E Barton, B C Davison, et al.
Human Mutation|October 29, 2002
The detection of large deletions or duplications in genomic DNAJ A L Armour, D E Barton, D J Cockburn, et al.
Nature Reviews. Genetics|September 5, 2001
Quality control in molecular genetic testingE Dequeker, S Ramsden, W W Grody, et al.
Oncogene Research|January 1, 1988
Chromosomal mapping of genes for transforming growth factors beta 2 and beta 3 in man and mouse: dispersion of TGF-beta gene familyD E Barton, B E Foellmer, J Du, et al.
Human Molecular Genetics|February 1, 1995
Haplotype analysis of the delta 2642 and (CAG)n polymorphisms in the Huntington's disease (HD) gene provides an explanation for an apparent 'founder' HD haplotypeD C Rubinsztein, J Leggo, S Goodburn, et al.
Pageof 7

Showing results (11-20 of 65) with videos related to

Sort By:
Pageof 7
Genomics|October 1, 1989
Level of expression and chromosome mapping of the mouse cholecystokinin gene: implications for murine models of genetic obesityJ M Friedman, B S Schneider, D E Barton, et al.
Genomics|October 1, 1987
The myelin-associated glycoprotein gene: mapping to human chromosome 19 and mouse chromosome 7 and expression in quivering miceD E Barton, M Arquint, J Roder, et al.
Neurology|July 27, 2005
Fragile X-associated tremor/ataxia syndrome presenting in a woman after chemotherapyJ P O'Dwyer, C Clabby, J Crown, et al.
Nature Genetics|November 1, 1993
Site of (CCG) polymorphism in the HD geneD C Rubinsztein, J Leggo, D E Barton, et al.
Journal of Medical Genetics|October 1, 1994
Chimaerism shown by cytogenetics and DNA polymorphism analysisA J Green, D E Barton, P Jenks, et al.
Human Molecular Genetics|October 1, 1993
Analysis of the huntingtin gene reveals a trinucleotide-length polymorphism in the region of the gene that contains two CCG-rich stretches and a correlation between decreased age of onset of Huntington's disease and CAG repeat numberD C Rubinsztein, D E Barton, B C Davison, et al.
Human Mutation|October 29, 2002
The detection of large deletions or duplications in genomic DNAJ A L Armour, D E Barton, D J Cockburn, et al.
Nature Reviews. Genetics|September 5, 2001
Quality control in molecular genetic testingE Dequeker, S Ramsden, W W Grody, et al.
Oncogene Research|January 1, 1988
Chromosomal mapping of genes for transforming growth factors beta 2 and beta 3 in man and mouse: dispersion of TGF-beta gene familyD E Barton, B E Foellmer, J Du, et al.
Human Molecular Genetics|February 1, 1995
Haplotype analysis of the delta 2642 and (CAG)n polymorphisms in the Huntington's disease (HD) gene provides an explanation for an apparent 'founder' HD haplotypeD C Rubinsztein, J Leggo, S Goodburn, et al.
Pageof 7