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

Jongmans, M.; Kuiper, R.; Carmichael, C.; Wilkins, E.; Dors, N.; Carmagnac, A.; Schouten-van Meeteren, N.; Li, X.; Stankovic, M.; Kamping, E.; Bengtsson, H.; Schoenmakers, M.; Geurts van Kessel, A.; Hoogerbrugge, P.; Hahn, C.; Brons, P.; Scott, H.; Hoogerbrugge, N.

doi:10.1038/leu.2009.210

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

Date

2010

Authors

Jongmans, M.

Kuiper, R.

Carmichael, C.

Wilkins, E.

Dors, N.

Carmagnac, A.

Schouten-van Meeteren, N.

Li, X.

Stankovic, M.

Kamping, E.

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Journal article

Citation

Leukemia, 2010; 24(1):242-246

Statement of Responsibility

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

DOI

10.1038/leu.2009.210

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Published Version

https://doi.org/10.1038/leu.2009.210

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http://hdl.handle.net/2440/62193

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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

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