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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Publisher’s version
Publication year
2010Author(s)
Source
Leukemia, 24, 1, (2010), pp. 242-6ISSN
Annotation
01 januari 2010
Publication type
Article / Letter to editor
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Organization
Human Genetics
Paediatrics - OUD tm 2017
Medical Oncology
Journal title
Leukemia
Volume
vol. 24
Issue
iss. 1
Page start
p. 242
Page end
p. 6
Subject
NCEBP 1: Molecular epidemiology; NCMLS 6: Genetics and epigenetic pathways of disease; ONCOL 1: Hereditary cancer and cancer-related syndromesThis item appears in the following Collection(s)
- Academic publications [238441]
- Electronic publications [122544]
- Faculty of Medical Sciences [90373]
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