Hidden chromosomal aberrations are rare in primary myelodysplastic syndromes with evolution to acute myeloid leukaemia and normal cytogenetics

This publication has 22 references indexed in Scilit:

• Primary myelodysplastic syndrome with normal cytogenetics: utility of ‘FISH panel testing’ and M-FISH
  Leukemia Research, 2002
• Trisomy 8 and monosomy 7 detected in bone marrow using primed in situ labeling, fluorescence in situ hybridization, and conventional cytogenetic analyses.
  Cancer Genetics and Cytogenetics, 2001
• An Optimized Set of Human Telomere Clones for Studying Telomere Integrity and Architecture
  American Journal of Human Genetics, 2000
• Incidence, characterization and prognostic significance of chromosomal abnormalities in 640 patients with primary myelodysplastic syndromes
  British Journal of Haematology, 2000
• Genetic Alterations in Hormone-Refractory Recurrent Prostate Carcinomas
  The American Journal of Pathology, 1998
• Hidden monosomy 7 in acute myeloid leukemia and myelodysplastic syndrome detected by interphase fluorescence in situ hybridization
  Leukemia Research, 1996
• Diagnostic and Prognostic Significance of Cytogenetics in Adult Primary Myelodysplastic Syndromes
  Leukemia & Lymphoma, 1996
• Cytogenetic and molecular delineation of the smallest commonly deleted region of chromosome 5 in malignant myeloid diseases.
  Proceedings of the National Academy of Sciences, 1993
• Specific metaphase and interphase detection of the breakpoint region in 8q24 of burkitt lymphoma cells by triple‐color fluorescence in situ hybridization
  Genes, Chromosomes and Cancer, 1992
• Labeling deoxyribonucleic acid to high specific activity in vitro by nick translation with DNA polymerase I
  Journal of Molecular Biology, 1977