PTPN11 mutations in childhood acute lymphoblastic leukemia occur as a secondary event associated with high hyperdiploidy

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Veröffentlicht in:	Leukemia 2010-01, Vol.24 (1), p.232-235
Hauptverfasser:	Molteni, C G, te Kronnie, G, Bicciato, S, Villa, T, Tartaglia, M, Basso, G, Biondi, A, Cazzaniga, G
Format:	Artikel
Sprache:	eng
Schlagworte:	Acute lymphocytic leukemia Biological and medical sciences Cancer Research Child Critical Care Medicine Diploidy Genes, ras Genetic aspects Health aspects Hematologic and hematopoietic diseases Hematology Humans Intensive Internal Medicine letter-to-the-editor Leukemia in children Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis Medical sciences Medicine Medicine & Public Health Mutation Oncology Phosphatases Polymerase Chain Reaction Polymorphism, Single Nucleotide Precursor Cell Lymphoblastic Leukemia-Lymphoma - genetics Protein Tyrosine Phosphatase, Non-Receptor Type 11 - genetics Risk factors
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