dc.contributor.author | Burford, A | |
dc.contributor.author | Mackay, A | |
dc.contributor.author | Popov, S | |
dc.contributor.author | Vinci, M | |
dc.contributor.author | Carvalho, D | |
dc.contributor.author | Clarke, M | |
dc.contributor.author | Izquierdo, E | |
dc.contributor.author | Avery, A | |
dc.contributor.author | Jacques, TS | |
dc.contributor.author | Ingram, WJ | |
dc.contributor.author | Moore, AS | |
dc.contributor.author | Frawley, K | |
dc.contributor.author | Hassall, TE | |
dc.contributor.author | Robertson, T | |
dc.coverage.spatial | Denver, CO | |
dc.date.accessioned | 2018-01-24T16:00:17Z | |
dc.date.issued | 2018-06-01 | |
dc.identifier | http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000438339000058&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=d4b848928d1c3e5c86d298abb68475f9 | |
dc.identifier.citation | NEURO-ONCOLOGY, 2018, 20 pp. 40 - 40 (1) | |
dc.identifier.issn | 1522-8517 | |
dc.identifier.uri | https://repository.icr.ac.uk/handle/internal/1027 | |
dc.identifier.eissn | 1523-5866 | |
dc.format.extent | 40 - 40 (1) | |
dc.language | eng | |
dc.language.iso | eng | |
dc.publisher | OXFORD UNIV PRESS INC | |
dc.rights.uri | https://creativecommons.org/licenses/by/4.0 | |
dc.subject | Science & Technology | |
dc.subject | Life Sciences & Biomedicine | |
dc.subject | Oncology | |
dc.subject | Clinical Neurology | |
dc.subject | Neurosciences & Neurology | |
dc.title | THE TEN-YEAR EVOLUTIONARY TRAJECTORY OF A HIGHLY RECURRENT PAEDIATRIC HIGH GRADE NEUROEPITHELIAL TUMOUR WITH MN1:BEND2 FUSION | |
dc.type | Journal Article | |
dcterms.dateAccepted | 2017-12-29 | |
rioxxterms.licenseref.uri | https://creativecommons.org/licenses/by/4.0 | |
rioxxterms.licenseref.startdate | 2018-06-01 | |
rioxxterms.type | Journal Article/Review | |
dc.relation.isPartOf | NEURO-ONCOLOGY | |
pubs.notes | Not known | |
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/Cancer Therapeutics | |
pubs.organisational-group | /ICR/Primary Group/ICR Divisions/Cancer Therapeutics/Glioma Team | |
pubs.organisational-group | /ICR/Primary Group/ICR Divisions/Molecular Pathology | |
pubs.organisational-group | /ICR/Primary Group/ICR Divisions/Molecular Pathology/Glioma Team | |
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/Cancer Therapeutics | |
pubs.organisational-group | /ICR/Primary Group/ICR Divisions/Cancer Therapeutics/Glioma Team | |
pubs.organisational-group | /ICR/Primary Group/ICR Divisions/Molecular Pathology | |
pubs.organisational-group | /ICR/Primary Group/ICR Divisions/Molecular Pathology/Glioma Team | |
pubs.publication-status | Published | |
pubs.volume | 20 | |
pubs.embargo.terms | Not known | |
icr.researchteam | Glioma Team | |
dc.contributor.icrauthor | Mackay, Alan | |
dc.contributor.icrauthor | Clarke, Matthew | |