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dc.contributor.authorPoddighe, PJen_US
dc.contributor.authorVeening, MAen_US
dc.contributor.authorMansur, MBen_US
dc.contributor.authorLoonen, AHen_US
dc.contributor.authorWesters, TMen_US
dc.contributor.authorMerle, PAen_US
dc.contributor.authorWessels, JWen_US
dc.contributor.authorde Haas, Ven_US
dc.contributor.authorKors, WAen_US
dc.contributor.authorBhola, SLen_US
dc.contributor.authorWondergem, MJen_US
dc.contributor.authorFord, AMen_US
dc.contributor.authorKaspers, GJLen_US
dc.date.accessioned2020-08-04T15:00:16Z
dc.date.issued2018-03
dc.identifier.citationHuman Pathology: Case Reports, 2018, 11 pp. 34 - 38
dc.identifier.issn2214-3300
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/3895
dc.identifier.doi10.1016/j.ehpc.2017.09.001
dc.format.extent34 - 38
dc.languageeng
dc.language.isoeng
dc.publisherElsevier BV
dc.rights.urihttps://creativecommons.org/licenses/by/4.0
dc.titleA novel cryptic CBFB-MYH11 gene fusion present at birth leading to acute myeloid leukemia and allowing molecular monitoring for minimal residual disease
dc.typeJournal Article
dcterms.dateAccepted2017-09-05
rioxxterms.versionofrecord10.1016/j.ehpc.2017.09.001
rioxxterms.licenseref.urihttps://creativecommons.org/licenses/by-nc-nd/4.0
rioxxterms.licenseref.startdate2018-03
rioxxterms.typeJournal Article/Review
dc.relation.isPartOfHuman Pathology: Case Reportsen_US
pubs.notesNo embargo
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Molecular Pathology
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Molecular Pathology/Biology of Childhood Leukaemia
pubs.publication-statusPublished
pubs.volume11en_US
pubs.embargo.termsNo embargo
icr.researchteamBiology of Childhood Leukaemiaen_US
dc.contributor.icrauthorFord, Anthonyen


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