Fluorescence in situ hybridization and conventional cytogenetics for the diagnosis of 11q23+ /mll + translocation in leukaemia
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2141.2003.04382.x/fullpdf
Reference8 articles.
1. A DNA probe combination for improved detection of MLL/11q23 breakpoints by double-color interphase-FISH in acute leukemias;Von Bergh;Genes Chromosomes and Cancer,2000
2. Comparison of cytogenetics and molecular cytogenetic detection of chromosome abnormalities in 240 consecutive adult patients with acute myeloid leukemia;Frohling;Journal of Clinical Oncology,2002
3. Distinct genetic patterns can be identified in acute monoblastic and acute moncytic leukaemia (FAB AML M5a and M5b): a study of 124 patients;Haferlach;British Journal of Haematology,2002
4. 11q23 abnormalities in patients with acute myelogenous leukemia and myelodysplastic syndrome as detected by molecular and cytogenetic analyses;Ibrahim;American Journal of Clinical Pathology,2000
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