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J D Brook

Showing results (41-50 of 72) with videos related to

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Journal of Medical Genetics|March 1, 1993
A study of DNA methylation in myotonic dystrophyD J Shaw, S Chaudhary, S A Rundle, et al.
Human Genetics|January 1, 1985
The apolipoprotein CII gene: subchromosomal localisation and linkage to the myotonic dystrophy locusD J Shaw, A L Meredith, M Sarfarazi, et al.
Nucleic Acids Research|February 25, 1990
A HindIII polymorphism identified by a DNA clone which maps to chromosome 17 (D17S245)J D Brook, M Upadhyaya, W Broadhead, et al.
Journal of Medical Genetics|November 1, 1992
Minimal expression of myotonic dystrophy: a clinical and molecular analysisW Reardon, H G Harley, J D Brook, et al.
Human Genetics|August 1, 1990
Linkage relationships of the apolipoprotein C1 gene and a cytochrome P450 gene (CYP2A) to myotonic dystrophyK V Walsh, H G Harley, J D Brook, et al.
Somatic Cell and Molecular Genetics|March 1, 1991
Stem cell factor (SCF), a novel hematopoietic growth factor and ligand for c-kit tyrosine kinase receptor, maps on human chromosome 12 between 12q14.3 and 12qterE N Geissler, M Liao, J D Brook, et al.
Nucleic Acids Research|July 11, 1988
A novel human cytochrome P450 gene (P450IIB): chromosomal localization and evidence for alternative splicingJ S Miles, N K Spurr, A C Gough, et al.
Nature Genetics|April 1, 1994
Holt-Oram syndrome is a genetically heterogeneous disease with one locus mapping to human chromosome 12qJ A Terrett, R Newbury-Ecob, G S Cross, et al.
Human Genetics|January 1, 1985
Assignment of human ferritin genes to chromosomes 11 and 19q13.3----19qterM Worwood, J D Brook, S J Cragg, et al.
Lancet (London, England)|May 9, 1992
Unstable DNA sequence in myotonic dystrophyH G Harley, S A Rundle, W Reardon, et al.
Pageof 8

Showing results (41-50 of 72) with videos related to

Sort By:
Pageof 8
Journal of Medical Genetics|March 1, 1993
A study of DNA methylation in myotonic dystrophyD J Shaw, S Chaudhary, S A Rundle, et al.
Human Genetics|January 1, 1985
The apolipoprotein CII gene: subchromosomal localisation and linkage to the myotonic dystrophy locusD J Shaw, A L Meredith, M Sarfarazi, et al.
Nucleic Acids Research|February 25, 1990
A HindIII polymorphism identified by a DNA clone which maps to chromosome 17 (D17S245)J D Brook, M Upadhyaya, W Broadhead, et al.
Journal of Medical Genetics|November 1, 1992
Minimal expression of myotonic dystrophy: a clinical and molecular analysisW Reardon, H G Harley, J D Brook, et al.
Human Genetics|August 1, 1990
Linkage relationships of the apolipoprotein C1 gene and a cytochrome P450 gene (CYP2A) to myotonic dystrophyK V Walsh, H G Harley, J D Brook, et al.
Somatic Cell and Molecular Genetics|March 1, 1991
Stem cell factor (SCF), a novel hematopoietic growth factor and ligand for c-kit tyrosine kinase receptor, maps on human chromosome 12 between 12q14.3 and 12qterE N Geissler, M Liao, J D Brook, et al.
Nucleic Acids Research|July 11, 1988
A novel human cytochrome P450 gene (P450IIB): chromosomal localization and evidence for alternative splicingJ S Miles, N K Spurr, A C Gough, et al.
Nature Genetics|April 1, 1994
Holt-Oram syndrome is a genetically heterogeneous disease with one locus mapping to human chromosome 12qJ A Terrett, R Newbury-Ecob, G S Cross, et al.
Human Genetics|January 1, 1985
Assignment of human ferritin genes to chromosomes 11 and 19q13.3----19qterM Worwood, J D Brook, S J Cragg, et al.
Lancet (London, England)|May 9, 1992
Unstable DNA sequence in myotonic dystrophyH G Harley, S A Rundle, W Reardon, et al.
Pageof 8