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Springer Nature [academic journals on nature.com], Leukemia, 1(24), p. 242-246, 2009

DOI: 10.1038/leu.2009.210

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

Journal article published in 2009 by M. C. J. Jongmans, R. P. Kuiper, C. L. Carmichael, E. J. Wilkins, N. Dors, A. Carmagnac, N. Schouten-Van Meeteren, A. Y. N. Schouten-Van Meeteren, X. Li, M. Stankovic, E. J. Kamping, H. Bengtsson, A. Geurts van Kessel, E. F. P. M. Schoenmakers, A. H. M. Geurts van Kessel and other authors.
This paper is made freely available by the publisher.
This paper is made freely available by the publisher.

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Abstract

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