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

M. C J Jongmans, R. P. Kuiper, C. L. Carmichael, Ella J Wilkins, N. Dors, Amandine Carmagnac, A. Y N Schouten-Van Meeteren, X. Li, M. Stankovic, E. Kamping, Henrik Bengtsson, E. F P M Schoenmakers, A Geurts van Kessel, P. M. Hoogerbrugge, Christopher N Hahn, P. P. Brons, H. S. Scott, N. Hoogerbrugge

Research output: Contribution to journalLetterOtherpeer-review

61 Citations (Scopus)
Original languageEnglish
Pages (from-to)242-246
Number of pages5
Issue number1
Publication statusPublished - Jan 2010
Externally publishedYes

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