articleTop 1% cited

High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays

Nature Genetics · 1998 · Vol. 20(2) · pp. 207–211

Daniel Pinkel✉(Cancer Genetics (United States))Richard Segraves(University of California, San Francisco)Damir Sudar(Lawrence Berkeley National Laboratory)Steven M. Clark(Cancer Genetics (United States))Ian Poole(Abbott (United Kingdom))David Kowbel(Lawrence Berkeley National Laboratory)Colin C. Collins(Lawrence Berkeley National Laboratory)Wen-Lin Kuo(University of California, San Francisco)Chira Chen(Cancer Genetics (United States))Y Zhai(University of California, San Francisco)Shanaz H. Dairkee(Cancer Research Institute)Britt‐Marie Ljung(University of California, San Francisco)Joe W. Gray(Cancer Genetics (United States))Donna G. Albertson(Cancer Genetics (United States))

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Genomic variations and chromosomal abnormalities Microtubule and mitosis dynamics Prenatal Screening and DiagnosticsBiologyComparative genomic hybridizationCopy-number variationGeneticsLocus (genetics)Gene dosageGenomeCopy number analysisMetaphaseHuman genome

MeSH terms

AnimalsBreast NeoplasmsChromosome AberrationsDNAFemaleGenetic MarkersHumansMicrochemistryNucleic Acid HybridizationTumor Cells, CulturedX ChromosomeIn Situ Hybridization, FluorescenceGene DosageMice

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Structural variation in the human genome