Please use this identifier to cite or link to this item: http://bura.brunel.ac.uk/handle/2438/19006
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dc.contributor.authorBeaney, KE-
dc.contributor.authorCooper, JA-
dc.contributor.authorDrenos, F-
dc.contributor.authorHumphries, SE-
dc.date.accessioned2019-08-27T10:26:24Z-
dc.date.available2017-10-01-
dc.date.available2019-08-27T10:26:24Z-
dc.date.issued2016-06-06-
dc.identifier.citationClinical Chemistry and Laboratory Medicine, 2017, 55 (10), pp. 1605 - 1613en_US
dc.identifier.issn1434-6621-
dc.identifier.issnhttp://dx.doi.org/10.1515/cclm-2016-0984-
dc.identifier.issn1437-4331-
dc.identifier.urihttp://bura.brunel.ac.uk/handle/2438/19006-
dc.description.sponsorshipUK Medical Research Council; British Heart Foundation;en_US
dc.format.extent1605 - 1613-
dc.language.isoenen_US
dc.publisherDe Gruyteren_US
dc.subjectCoronary heart disease;en_US
dc.subjectGenetic risk;en_US
dc.subjectRisk predictionen_US
dc.titleAssessment of the clinical utility of adding common single nucleotide polymorphism genetic scores to classical risk factor algorithms in coronary heart disease risk prediction in UK menen_US
dc.typeArticleen_US
dc.identifier.doihttp://dx.doi.org/10.1515/cclm-2016-0984-
dc.relation.isPartOfClinical Chemistry and Laboratory Medicine-
pubs.issue10-
pubs.publication-statusPublished-
pubs.volume55-
dc.identifier.eissn1437-4331-
Appears in Collections:Dept of Life Sciences Research Papers

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