Burkitt t(8;14)(q24;q32) and cryptic deletion in a CLL patient: report of a case and review of literature

This publication has 26 references indexed in Scilit:

• Molecular genetics and its clinical relevance
  Hematology/Oncology Clinics of North America, 2004
• Chromosome anomalies detected by interphase fluorescence in situ hybridization: correlation with significant biological features of B‐cell chronic lymphocytic leukaemia
  British Journal of Haematology, 2003
• Multivariate analysis of prognostic factors in CLL: clinical stage, IGVH gene mutational status, and loss or mutation of the p53 gene are independent prognostic factors
  Blood, 2002
• Genomic Aberrations and Survival in Chronic Lymphocytic Leukemia
  New England Journal of Medicine, 2000
• Occurrence of both t(1;19) and t(8;14) in a Patient with Chronic Lymphocytic Leukemia
  Experimental and Molecular Pathology, 1999
• Chromosome aberrations in B-cell chronic lymphocytic leukemia: reassessment based on molecular cytogenetic analysis
  Journal of Molecular Medicine, 1999
• Prognostic Subgroups in B-Cell Chronic Lymphocytic Leukemia Defined by Specific Chromosomal Abnormalities
  New England Journal of Medicine, 1990
• Consistency of chromosomal aberrations in chronic B-lymphocytic leukemia. A longitudinal cytogenetic study of 41 patients
  Cancer, 1988
• There are differences in cytogenetic abnormalities among histologic subtypes of the non-Hodgkin's lymphomas
  Blood, 1985
• Karyotype peculiarities of malignant lymphomas
  Human Genetics, 1977