Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/62193
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Type: Journal article
Title: Novel RUNX1 mutations in familial platelet disorder with enhanced risk for acute myeloid leukemia: clues for improved identification of the FPD/AML syndrome
Author: Jongmans, M.
Kuiper, R.
Carmichael, C.
Wilkins, E.
Dors, N.
Carmagnac, A.
Schouten-van Meeteren, N.
Li, X.
Stankovic, M.
Kamping, E.
Bengtsson, H.
Schoenmakers, M.
Geurts van Kessel, A.
Hoogerbrugge, P.
Hahn, C.
Brons, P.
Scott, H.
Hoogerbrugge, N.
Citation: Leukemia, 2010; 24(1):242-246
Publisher: Nature Publishing Group
Issue Date: 2010
ISSN: 0887-6924
1476-5551
Statement of
Responsibility: 
MCJ Jongmans, RP Kuiper, CL Carmichael, EJ Wilkins, N Dors, A Carmagnac, AYN Schouten-van Meeteren, X Li, M Stankovic, E Kamping, H Bengtsson, EFPM Schoenmakers, A Geurts van Kessel, PM Hoogerbrugge, CN Hahn, PP Brons, HS Scott and N Hoogerbrugge
Keywords: Humans
Blood Platelet Disorders
Gene Deletion
Mutation
Child
Child, Preschool
Female
Male
Core Binding Factor Alpha 2 Subunit
Leukemia, Myeloid, Acute
Rights: © 2010 Nature Publishing Group
DOI: 10.1038/leu.2009.210
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