t(4;11) translocation in hyperdiploid de novo adult acute myeloid leukemia: A case report
Author:
Publisher
Baishideng Publishing Group Inc.
Subject
General Medicine
Reference29 articles.
1. Identification of a gene, MLL, that spans the breakpoint in 11q23 translocations associated with human leukemias.
2. 11q23 Abnormalities in Patients With Acute Myelogenous Leukemia and Myelodysplastic Syndrome as Detected by Molecular and Cytogenetic Analyses
3. AML with 11q23/MLL abnormalities as defined by the WHO classification: incidence, partner chromosomes, FAB subtype, age distribution, and prognostic impact in an unselected series of 1897 cytogenetically analyzed AML cases
4. Refinement of cytogenetic classification in acute myeloid leukemia: determination of prognostic significance of rare recurring chromosomal abnormalities among 5876 younger adult patients treated in the United Kingdom Medical Research Council trials
5. Fluorescence in situ hybridization and conventional cytogenetics for the diagnosis of 11q23+ /mll + translocation in leukaemia
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