Increased C-MYC Oncogene Copy Number Detected with Combined Modified Comparative Genomic Hybridization and FISH Analysis in a Richter Syndrome Case with Complex Karyotype
- 1 October 1998
- journal article
- case report
- Published by Elsevier in Cancer Genetics and Cytogenetics
- Vol. 106 (1) , 80-83
- https://doi.org/10.1016/s0165-4608(98)00037-5
Abstract
No abstract availableKeywords
This publication has 14 references indexed in Scilit:
- Richter's syndrome in a case of atypical chronic lymphocytic leukaemia with the t(11;14)(q13;q32): role for a p53 exon 7 gene mutationBritish Journal of Haematology, 1996
- Identification of amplified DNA sequences in breast cancer and their organization within homogeneously staining regionsGenes, Chromosomes and Cancer, 1995
- Comparative genomic hybridization in acute myeloid leukemia: A comparison with G-banding and chromosome paintingCancer Genetics and Cytogenetics, 1995
- Detection of DNA amplification in 17 primary breast carcinomas with homogeneously staining regions by a modified comparative genomic hybridization techniqueGenes, Chromosomes and Cancer, 1994
- Cytogenetic studies in patients with Richter's syndromeCancer Genetics and Cytogenetics, 1994
- Molecular genetic demonstration of the diverse evolution of Richter's syndrome (chronic lymphocytic leukemia and subsequent large cell lymphoma)Blood, 1994
- Serial phenotypic, cytogenetic and molecular genetic studies in Richter's syndrome: demonstration of lymphoma development from the chronic lymphocytic leukaemia cellsBritish Journal of Haematology, 1993
- p53 mutations in human lymphoid malignancies: association with Burkitt lymphoma and chronic lymphocytic leukemia.Proceedings of the National Academy of Sciences, 1991
- Inactivation of the retinoblastoma gene in human lymphoid neoplasmsBlood, 1991
- A RAPID BANDING TECHNIQUE FOR HUMAN CHROMOSOMESThe Lancet, 1971