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D J Cockburn

Showing results (1-10 of 9) with videos related to

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Methods in Molecular Medicine|March 5, 2011
Pulsed field gel electrophoresis for detection of gene rearrangements in duchenne muscular dystrophyD J Cockburn, A Seller
Basic Life Sciences|January 1, 1985
Meiotic investigations of aneuploidy in the humanM Hulten, N Saadallah, B M Wallace, et al.
Human Genetics|December 1, 1992
Mapping of X chromosome translocation breakpoints in females with Duchenne muscular dystrophy with respect to exons of the dystrophin geneD J Cockburn, E A Munro, I W Craig, et al.
Nucleic Acids Research|January 11, 1991
Two RFLPs at the D12S51 locusR Newton, D J Henderson, D J Cockburn, 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.
Cytogenetics and Cell Genetics|January 1, 1992
Assignment of apolipoprotein H (APOH: beta-2-glycoprotein I) to human chromosome 17q23----qter; determination of the major expression siteA Steinkasserer, D J Cockburn, D M Black, et al.
Nucleic Acids Research|March 11, 1991
A dinucleotide repeat polymorphism at the DMD locusJ F Powell, F H Fodor, D J Cockburn, et al.
Gene|November 14, 1998
Is gene deletion in eukaryotes sequence-dependent? A study of nine deletion junctions and nineteen other deletion breakpoints in intron 7 of the human dystrophin geneJ C McNaughton, D J Cockburn, G Hughes, et al.
Molecular and Cellular Probes|October 1, 1995
Molecular characterization of further dystrophin gene microsatellitesS C King, A L Roche, M R Passos-Bueno, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Methods in Molecular Medicine|March 5, 2011
Pulsed field gel electrophoresis for detection of gene rearrangements in duchenne muscular dystrophyD J Cockburn, A Seller
Basic Life Sciences|January 1, 1985
Meiotic investigations of aneuploidy in the humanM Hulten, N Saadallah, B M Wallace, et al.
Human Genetics|December 1, 1992
Mapping of X chromosome translocation breakpoints in females with Duchenne muscular dystrophy with respect to exons of the dystrophin geneD J Cockburn, E A Munro, I W Craig, et al.
Nucleic Acids Research|January 11, 1991
Two RFLPs at the D12S51 locusR Newton, D J Henderson, D J Cockburn, 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.
Cytogenetics and Cell Genetics|January 1, 1992
Assignment of apolipoprotein H (APOH: beta-2-glycoprotein I) to human chromosome 17q23----qter; determination of the major expression siteA Steinkasserer, D J Cockburn, D M Black, et al.
Nucleic Acids Research|March 11, 1991
A dinucleotide repeat polymorphism at the DMD locusJ F Powell, F H Fodor, D J Cockburn, et al.
Gene|November 14, 1998
Is gene deletion in eukaryotes sequence-dependent? A study of nine deletion junctions and nineteen other deletion breakpoints in intron 7 of the human dystrophin geneJ C McNaughton, D J Cockburn, G Hughes, et al.
Molecular and Cellular Probes|October 1, 1995
Molecular characterization of further dystrophin gene microsatellitesS C King, A L Roche, M R Passos-Bueno, et al.
Pageof 1