Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/68193
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dc.contributor.authorFletcher, L.-
dc.contributor.authorPrime, J.-
dc.contributor.authorPhillis, S.-
dc.contributor.authorJamison, B.-
dc.contributor.authorField, C.-
dc.contributor.authorPrime, H.-
dc.contributor.authorSullivan, B.-
dc.contributor.authorYeoman, A.-
dc.contributor.authorGeorgievski, J.-
dc.contributor.authorParker, W.-
dc.contributor.authorSlader, C.-
dc.contributor.authorHughes, T.-
dc.contributor.authorBranford, S.-
dc.date.issued2010-
dc.identifier.citationProceedings of Haematology Association of Australasia Annual Meeting, 2010;-
dc.identifier.urihttp://hdl.handle.net/2440/68193-
dc.description.statementofresponsibilityLinda Fletcher, Jodi Prime, Stuart Phillis, Bronte Jamison, Chani Field, Haley Prime, Brad Sullivan, Alexandra Yeoman, Jasmina Georgievski, Wendy Parker, Cassandra Slader, Timothy Hughes, Susan Branford-
dc.language.isoen-
dc.rightsCopyright status unknown-
dc.titleLimiting the variability within a BCR-ABL quantitative PCR (RQ-PCR) assay is essential for optimal concordance of results between laboratories generating BCR-ABL values on an international reporting scale-
dc.typeConference paper-
dc.contributor.conferenceHaematology Association of Australasia Annual Meeting (2010 : Auckland, New Zealand)-
pubs.publication-statusPublished-
dc.identifier.orcidHughes, T. [0000-0002-0910-3730] [0000-0002-7990-4509]-
dc.identifier.orcidBranford, S. [0000-0002-1964-3626] [0000-0002-5095-7981]-
Appears in Collections:Aurora harvest 5
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