Implementation of array based whole-genome high-resolution technologies confirms the absence of secondary copy-number alterations in MLL-AF4-positive infant ALL patients

Gespeichert in:

Bibliographische Detailangaben
Veröffentlicht in:	Leukemia 2011-01, Vol.25 (1), p.175-178
Hauptverfasser:	Bardini, M, Galbiati, M, Lettieri, A, Bungaro, S, Gorletta, T A, Biondi, A, Cazzaniga, G
Format:	Artikel
Sprache:	eng
Schlagworte:	692/420/2489/68 692/699/67/1990/283/2125 Biological and medical sciences Cancer in children Cancer Research Chromosome Aberrations Critical Care Medicine Gene Dosage Genetic aspects Hematologic and hematopoietic diseases Hematology Humans Indexing in process Infant Intensive Internal Medicine letter-to-the-editor Leukemia Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis Loss of Heterozygosity Medical genetics Medical sciences Medicine Medicine & Public Health Myeloid-Lymphoid Leukemia Protein - analysis Oligonucleotide Array Sequence Analysis - methods Oncogene Proteins, Fusion - analysis Oncology Polymorphism, Single Nucleotide Precursor Cell Lymphoblastic Leukemia-Lymphoma - genetics
Online-Zugang:	Volltext
Tags:	Tag hinzufügen Keine Tags, Fügen Sie den ersten Tag hinzu!