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dc.contributor.authorHenaghan, Mark
dc.contributor.authorCho, Mildred K.
dc.date.available2018-11-29T21:13:10Z
dc.date.copyright2007
dc.identifier.citationGENES, SOCIETY AND THE FUTURE, Vol. I, Part 5, Human Genome Research Project, Dunedin, NZ, 2007.en_NZ
dc.identifier.urihttp://hdl.handle.net/10523/8668
dc.description.abstractArray comparative genomic hybridisation (aCGH) represents a major advance in the field of cytogenetics and offers tremendous promise in prenatal diagnosis for the detection of genetic alterations leading to serious genetic conditions. This technology, also sometimes known as molecular karyotyping, can detect differences in DNA copy number at hundreds or thousands of points in the genome simultaneously. At this stage of the development of aCGH technology, a number of recommendations can be made for clinical use. These recommendations should be revisited as information about its clinical validity and utility is obtained, and as the accuracy, resolution and cost of aCGH-based tests evolve.en_NZ
dc.format.mimetypeapplication/pdf
dc.language.isoenen_NZ
dc.publisherThomson Reutersen_NZ
dc.relation.ispartofGenes, Society and the Futureen_NZ
dc.relation.ispartofseriesHuman Genome Research Projecten_NZ
dc.subjectGeneticsen_NZ
dc.subjectEthicsen_NZ
dc.subjectHuman genomeen_NZ
dc.subjectArray Comparative Genomic Hybridisationen_NZ
dc.titleArray Comparative Genomic Hybridisation (aCGH): An Analysis of the Current Technology and Its Future in Prenatal Diagnosisen_NZ
dc.typeChapter in Book
dc.date.updated2018-11-28T22:36:04Z
otago.schoolUniversity of Otago Faculty of Lawen_NZ
otago.openaccessOpenen_NZ
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