Occurrence of both t(1;19) and t(8;14) in a Patient with Chronic Lymphocytic Leukemia
- 31 August 1999
- journal article
- case report
- Published by Elsevier in Experimental and Molecular Pathology
- Vol. 66 (3) , 238-242
- https://doi.org/10.1006/exmp.1999.2267
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- Trisomy 10 in leukemiaCancer Genetics and Cytogenetics, 1998
- Translocation 2; 19 in a Patient with Probable Relapsed Acute Myeloid LeukemiaPathobiology, 1997
- Cytogenetic abnormalities in adult acute lymphoblastic leukemia: correlations with hematologic findings outcome. A Collaborative Study of the Group Francais de Cytogenetique Hematologique [published erratum appears in Blood 1996 Oct 1;88(7):2818]Blood, 1996
- The t(1;19)(q23;p13) results in consistent fusion of E2A and PBX1 coding sequences in acute lymphoblastic leukemiasBlood, 1991
- The Gene for Enhancer Binding Proteins E12/E47 Lies at the t(1;19) Breakpoint in Acute LeukemiasScience, 1989
- Translocation 1;19—A new cytogenetic abnormality in acute lymphocytic leukemiaCancer Genetics and Cytogenetics, 1984
- Pre-B cell leukemia associated with chromosome translocation 1;19Blood, 1984
- New chromosomal translocations correlate with specific immunophenotypes of childhood acute lymphoblastic leukemiaCell, 1984
- A RAPID BANDING TECHNIQUE FOR HUMAN CHROMOSOMESThe Lancet, 1971
- Chromosome preparations of leukocytes cultured from human peripheral bloodExperimental Cell Research, 1960