Original language | English |
---|---|
Pages (from-to) | 242-246 |
Number of pages | 5 |
Journal | Leukemia |
Volume | 24 |
Issue number | 1 |
DOIs | |
Publication status | Published - Jan 2010 |
Externally published | Yes |
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 journal › Letter › Other › peer-review
61
Citations
(Scopus)