A Novel Translocation (17;19)(p13;p13) in a Patient with Acute Myelomonocytic Leukemia
Author:
Publisher
Elsevier BV
Subject
Cancer Research,Genetics,Molecular Biology
Reference6 articles.
1. ISCN (1995): An International System for Human Cytogenetic Nomenclature. F Mitelman, ed. S. Karger, Basel.
2. Heterogeneity in the breakpoints of chromosome 19 among acute leukemic patients with the t(11;19)(q23;13) translocation;Mitani;Am J Hematol,1989
3. Translocation 2;19 in a patient with a probable relapsed acute myeloid leukemia;Mark;Pathobiology,1997
4. 17p deletion in acute myeloid leukemia and myelodyspastic syndrome. Analysis of breakpoints and deleted segments by fluorescence in situ;Soenen;Blood,1998
5. Acute myeloid leukemia and myelodysplastic syndromes following essential thrombocythemia treated with hydroxyurea;Sterkers;Blood,1998
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