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AuthorPort, Matthiasdc.contributor.author
AuthorBoettcher, Miriamdc.contributor.author
AuthorThol, Felicitasdc.contributor.author
AuthorTrachte, Nicoledc.contributor.author
AuthorWasem, Juergendc.contributor.author
AuthorGanser, Arnolddc.contributor.author
AuthorPouryamout, Lauradc.contributor.author
AuthorNeumann, Anjadc.contributor.author
Date of accession2020-02-19T13:57:58Zdc.date.accessioned
Available in OPARU since2020-02-19T13:57:58Zdc.date.available
Date of first publication2015dc.date.issued
Languageendc.language.iso
PublisherUniversität Ulmdc.publisher
KeywordMICRORNA EXPRESSION SIGNATURESdc.subject
KeywordNPM1 MUTATIONSdc.subject
KeywordNORMAL CYTOGENETICSdc.subject
KeywordCEBPA MUTATIONSdc.subject
KeywordADULT PATIENTSdc.subject
KeywordGENEdc.subject
KeywordCANCERdc.subject
KeywordPREVALENCEdc.subject
KeywordRELEVANCEdc.subject
KeywordPREDICTSdc.subject
Dewey Decimal GroupDDC 170 / Ethicsdc.subject.ddc
TitleIndividualised Medicine in the Diagnosis and Prognosis of Patients Younger than 65 Years with Normal Karyotype Acute Myeloid Leukemia: A Systematic Review and Meta-Analysis of the Impact of Fms-Related Tyrosine Kinase 3 Internal Tandem Duplication (FLT3-ITD)dc.title
Resource typeTeil eines Buchesdc.type
InstitutionInstitut für Radiobiologie der Bundeswehr in Verbindung mit der Universität Ulmuulm.affiliationSpecific
DCMI TypeTextuulm.typeDCMI
CategoryPublikationsnachweiseuulm.category
Source - Title of sourceEthics of personalised medicine: critical perspectivessource.title
Quellenangabe - HerausgeberVollmann, Jochensource.contributor.editor1
Source - PublisherOxfordsource.publisherPlace
Source - Place of publicationRoutledgesource.publisher
Source - Year2015source.year
Source - From page113source.fromPage
Source - To page127source.toPage
Source - ISBN978-1-315-61620-9source.identifier.isbn
Source - ISBN978-1-4724-4796-8source.identifier.isbn
CommunityWeitere Einrichtungenuulm.community
WoS000412854500010uulm.identifier.wos
Bibliographyuulmuulm.bibliographie


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