Mutation analysis for RUNX1, MLL-PTD, FLT3-ITD, NPM1 and NRAS in 269 patients with MDS or secondary AML

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Veröffentlicht in:	Leukemia 2010-08, Vol.24 (8), p.1528-1532
Hauptverfasser:	Dicker, F, Haferlach, C, Sundermann, J, Wendland, N, Weiss, T, Kern, W, Haferlach, T, Schnittger, S
Format:	Artikel
Sprache:	eng
Schlagworte:	631/208/1405 631/208/737 692/699/67/1990/1673 692/699/67/1990/283/1897 Aged Cancer Research Core Binding Factor Alpha 2 Subunit - genetics Critical Care Medicine Diagnosis Female fms-Like Tyrosine Kinase 3 - genetics Gene mutations Genes, ras Genetic aspects Health aspects Hematology Histone-Lysine N-Methyltransferase Humans Intensive Internal Medicine letter-to-the-editor Leukemia, Myeloid, Acute - genetics Male Medicine Medicine & Public Health Middle Aged Mutation Myelodysplastic syndromes Myelodysplastic Syndromes - genetics Myeloid-Lymphoid Leukemia Protein - genetics Nuclear Proteins - genetics Oncology Risk factors Runx1 protein
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