Translocation t(8;16)(p11;p13) in acute nonlymphoblastic leukemia (M4) possibly secondary to Hodgkin's disease
Author:
Publisher
Elsevier BV
Subject
Cancer Research,Genetics,Molecular Biology
Reference22 articles.
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2. A unique 8;16 translocation in two infants with poorly differentiated monoblastic leukemia;Bernstein;Cancer Genet Cytogenet,1987
3. Acute monoblastic leukemia with a single chromosomal rearrangement involving breakpoints on chromosome 8 and 16, 46,XX,t(8;16)(p11;p13);Juneja;Acta Haematol,1987
4. Chromosome patterns in 26 South African children with acute nonlymphocytic leukemia (ANLL);Bernstein;Cancer Genet Cytogenet,1984
5. Catalog of Chromosome Aberrations in Cancer;Mitelman,1985
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1. Karyotype Abnormalities in a Variant Chinese Hamster Cell Line Resistant to Methyl Methanesulphonate;Hereditas;2004-05-11
2. Secondary Acute Monocytic Leukemia with a Translocation t(8;16)(p11;p13): Case Report and Review of the Literature;Leukemia & Lymphoma;2004-03
3. Acute monoblastic leukemia with t(8;16): A distinct clinicopathologic entity; Report of a case and review of the literature;American Journal of Hematology;2001
4. RT-PCR analysis of theMOZ-CBP andCBP-MOZ chimeric transcripts in acute myeloid leukemias with t(8;16)(p11;p13);Genes, Chromosomes and Cancer;2000
5. 3p21 is a recurrent treatment-related breakpoint in myelodysplastic syndrome and acute myeloid leukemia;Cytogenetic and Genome Research;1996
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