(Q84962160)
Statements
Novel RUNX1 mutations in familial platelet disorder with enhanced risk for acute myeloid leukemia: clues for improved identification of the FPD/AML syndrome (English)
M C J Jongmans
R P Kuiper
E J Wilkins
N Dors
A Carmagnac
A Y N Schouten-van Meeteren
X Li
M Stankovic
E Kamping
H Bengtsson
E F P M Schoenmakers
A Geurts van Kessel
P M Hoogerbrugge
P P Brons
N Hoogerbrugge
15 October 2009