Skip to content
VuFind
    • English
    • Deutsch
    • Español
    • Français
    • Italiano
    • 日本語
    • Nederlands
    • Português
    • Português (Brasil)
    • 中文(简体)
    • 中文(繁體)
    • Türkçe
    • עברית
    • Gaeilge
    • Cymraeg
    • Ελληνικά
    • Català
    • Euskara
    • Русский
    • Čeština
    • Suomi
    • Svenska
    • polski
    • Dansk
    • slovenščina
    • اللغة العربية
    • বাংলা
    • Galego
    • Tiếng Việt
    • Hrvatski
    • हिंदी
    • Հայերէն
    • Українська
    • Sámegiella
    • Монгол
Advanced
  • FUNCTIONAL ANALYSES OF RUNX1 V...
  • Cite this
  • Text this
  • Email this
  • Print
  • Export Record
    • Export to RefWorks
    • Export to EndNoteWeb
    • Export to EndNote
  • Permanent link
FUNCTIONAL ANALYSES OF RUNX1 VARIANTS IN THE CONTEXT OF FAMILIAL PLATELET DISORDER WIT PREDISPOSITION TO HEMATOLOGIC MALIGNANCIES

FUNCTIONAL ANALYSES OF RUNX1 VARIANTS IN THE CONTEXT OF FAMILIAL PLATELET DISORDER WIT PREDISPOSITION TO HEMATOLOGIC MALIGNANCIES

Bibliographic Details
Main Authors: Melanie Decker, Förster Alisa, Prüne Alina, Anne Seebacher, Alena Wittstock, Thomas Illig, Brigitte Schlegelberger, Tim Ripperger
Format: Article
Language:English
Published: Elsevier 2023-12-01
Series:EJC Paediatric Oncology
Online Access:http://www.sciencedirect.com/science/article/pii/S2772610X2300048X
  • Holdings
  • Description
  • Similar Items
  • Staff View

Internet

http://www.sciencedirect.com/science/article/pii/S2772610X2300048X

Similar Items

  • SPECTRUM OF CLINICAL PHENOTYPES AND SOMATIC VARIANTS IN RUNX1-ASSOCIATED FAMILIAL PLATELET DISORDER WITH PREDISPOSITION TO HEMATOLOGIC MALIGNANCIES
    by: Alisa Förster, et al.
    Published: (2023-12-01)
  • Managing individuals with propensity to myeloid malignancies due to germline RUNX1 deficiency
    by: Tim Ripperger, et al.
    Published: (2011-12-01)
  • Familial platelet disorders with a predisposition to acute myelogenous leukaemia: a RUNX1 update
    by: Rossini J, et al.
    Published: (2012-04-01)
  • The clinical heterogeneity of RUNX1 associated familial platelet disorder with predisposition to myeloid malignancy – A case series and review of the literature
    by: Catherine Tang, et al.
    Published: (2020-01-01)
  • MDS1 and EVI1 complex locus (MECOM): a novel candidate gene for hereditary hematological malignancies
    by: Tim Ripperger, et al.
    Published: (2018-02-01)

Search Options

  • Search History
  • Advanced Search

Find More

  • Browse the Catalog
  • Browse Alphabetically
  • Explore Channels
  • Course Reserves
  • New Items

Need Help?

  • Search Tips
  • Ask a Librarian
  • FAQs