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

Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/62193

Scopus	Web of Science®	Altmetric
Citations
?	?

Type:	Journal article
Title:	Novel RUNX1 mutations in familial platelet disorder with enhanced risk for acute myeloid leukemia: clues for improved identification of the FPD/AML syndrome
Author:	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.
Citation:	Leukemia, 2010; 24(1):242-246
Publisher:	Nature Publishing Group
Issue Date:	2010
ISSN:	0887-6924 1476-5551
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
Keywords:	Humans Blood Platelet Disorders Gene Deletion Mutation Child Child, Preschool Female Male Core Binding Factor Alpha 2 Subunit Leukemia, Myeloid, Acute
Rights:	© 2010 Nature Publishing Group
DOI:	10.1038/leu.2009.210
Published version:	http://dx.doi.org/10.1038/leu.2009.210
Appears in Collections:	Aurora harvest Medicine publications

Files in This Item:

There are no files associated with this item.

Show full item record

Adelaide Research & Scholarship