Novel RUNX1 mutations in familial platelet disorder with enhanced risk for acute myeloid leukemia: clues for improved identification of the FPD/AML syndrome

Jongmans, MCJ; Kuiper, RP; Carmichael, CL; Wilkins, EJ; Dors, N; Carmagnac, A; Schouten-van Meeteren, AYN; Li, X; Stankovic, M; Kamping, E; Bengtsson, H; Schoenmakers, EFPM; van Kessel, AG; Hoogerbrugge, PM; Hahn, CN; Brons, PP; Scott, HS; Hoogerbrugge, N

Author(s): Jongmans, MCJ; Kuiper, RP; Carmichael, CL; Wilkins, EJ; Dors, N; Carmagnac, A; Schouten-van Meeteren, AYN; Li, X; Stankovic, M; Kamping, E; Bengtsson, H; Schoenmakers, EFPM; van Kessel, AG; Hoogerbrugge, PM; Hahn, CN; Brons, PP; Scott, HS; Hoogerbrugge, N;
Details: Publication Year 2010-01,Volume 24,Issue #1,Page 242-246
Journal Title: LEUKEMIA
Publication Type: Journal Article
Publisher: NATURE PUBLISHING GROUP
Keywords: ACUTE MYELOGENOUS LEUKEMIA; PROPENSITY
Publisher's Version: https://doi.org/10.1038/leu.2009.210
Terms of Use/Rights Notice: Refer to copyright notice on published article.

Creation Date: 2010-01-01 12:00:00