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Nigel P Carter

Showing results (21-30 of 104) with videos related to

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Genes, Chromosomes & Cancer|August 20, 2005
Deletion at chromosome band 20p12.1 in colorectal cancer revealed by high resolution array comparative genomic hybridizationEleanor J Davison, Patrick S Tarpey, Heike Fiegler, et al.
Nature Genetics|December 6, 2005
A high-resolution survey of deletion polymorphism in the human genomeDonald F Conrad, T Daniel Andrews, Nigel P Carter, et al.
European Journal of Human Genetics : EJHG|August 25, 2005
Molecular cytogenetic analyses of breakpoints in apparently balanced reciprocal translocations carried by phenotypically normal individualsJulia Baptista, Elena Prigmore, Susan M Gribble, et al.
Journal of Cell Science|May 15, 2008
Replication-timing-correlated spatial chromatin arrangements in cancer and in primate interphase nucleiFlorian Grasser, Michaela Neusser, Heike Fiegler, et al.
Human Genetics|November 19, 2004
A novel 5q11.2 deletion detected by microarray comparative genomic hybridisation in a child referred as a case of suspected 22q11 deletion syndromeKatrina Prescott, Kathryn Woodfine, Paula Stubbs, et al.
Clinical Dysmorphology|September 22, 2011
An atypical facial appearance and growth pattern in a child with Cornelia de Lange Syndrome: an intragenic deletion predicting loss of the N-terminal region of NIPBLJennie E Murray, Muhammed Walayat, Peter Gillett, et al.
Bioinformatics (Oxford, England)|March 2, 2011
aCGH.Spline--an R package for aCGH dye bias normalizationTomas W Fitzgerald, Lee D Larcombe, Solena Le Scouarnec, et al.
Nucleic Acids Research|December 21, 2006
High resolution array-CGH analysis of single cellsHeike Fiegler, Jochen B Geigl, Sabine Langer, et al.
The American Journal of Pathology|April 8, 2009
Sites of differential DNA methylation between placenta and peripheral blood: molecular markers for noninvasive prenatal diagnosis of aneuploidiesElisavet A Papageorgiou, Heike Fiegler, Vardhman Rakyan, et al.
Nature Genetics|December 7, 2007
Germline rates of de novo meiotic deletions and duplications causing several genomic disordersDaniel J Turner, Marcos Miretti, Diana Rajan, et al.
Pageof 11

Showing results (21-30 of 104) with videos related to

Sort By:
Pageof 11
Genes, Chromosomes & Cancer|August 20, 2005
Deletion at chromosome band 20p12.1 in colorectal cancer revealed by high resolution array comparative genomic hybridizationEleanor J Davison, Patrick S Tarpey, Heike Fiegler, et al.
Nature Genetics|December 6, 2005
A high-resolution survey of deletion polymorphism in the human genomeDonald F Conrad, T Daniel Andrews, Nigel P Carter, et al.
European Journal of Human Genetics : EJHG|August 25, 2005
Molecular cytogenetic analyses of breakpoints in apparently balanced reciprocal translocations carried by phenotypically normal individualsJulia Baptista, Elena Prigmore, Susan M Gribble, et al.
Journal of Cell Science|May 15, 2008
Replication-timing-correlated spatial chromatin arrangements in cancer and in primate interphase nucleiFlorian Grasser, Michaela Neusser, Heike Fiegler, et al.
Human Genetics|November 19, 2004
A novel 5q11.2 deletion detected by microarray comparative genomic hybridisation in a child referred as a case of suspected 22q11 deletion syndromeKatrina Prescott, Kathryn Woodfine, Paula Stubbs, et al.
Clinical Dysmorphology|September 22, 2011
An atypical facial appearance and growth pattern in a child with Cornelia de Lange Syndrome: an intragenic deletion predicting loss of the N-terminal region of NIPBLJennie E Murray, Muhammed Walayat, Peter Gillett, et al.
Bioinformatics (Oxford, England)|March 2, 2011
aCGH.Spline--an R package for aCGH dye bias normalizationTomas W Fitzgerald, Lee D Larcombe, Solena Le Scouarnec, et al.
Nucleic Acids Research|December 21, 2006
High resolution array-CGH analysis of single cellsHeike Fiegler, Jochen B Geigl, Sabine Langer, et al.
The American Journal of Pathology|April 8, 2009
Sites of differential DNA methylation between placenta and peripheral blood: molecular markers for noninvasive prenatal diagnosis of aneuploidiesElisavet A Papageorgiou, Heike Fiegler, Vardhman Rakyan, et al.
Nature Genetics|December 7, 2007
Germline rates of de novo meiotic deletions and duplications causing several genomic disordersDaniel J Turner, Marcos Miretti, Diana Rajan, et al.
Pageof 11