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dc.contributor.authorPoddighe, PJ
dc.contributor.authorVeening, MA
dc.contributor.authorMansur, MB
dc.contributor.authorLoonen, AH
dc.contributor.authorWesters, TM
dc.contributor.authorMerle, PA
dc.contributor.authorWessels, JW
dc.contributor.authorde Haas, V
dc.contributor.authorKors, WA
dc.contributor.authorBhola, SL
dc.contributor.authorWondergem, MJ
dc.contributor.authorFord, AM
dc.contributor.authorKaspers, GJL
dc.date.accessioned2020-08-04T15:00:16Z
dc.date.issued2018-03-01
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 Reports
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.volume11
pubs.embargo.termsNo embargo
icr.researchteamBiology of Childhood Leukaemia
dc.contributor.icrauthorFord, Anthony


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