The detection and significance of chromosomal abnormalities in childhood acute lymphoblastic leukaemia

This publication has 77 references indexed in Scilit:

• Monosomy 20 as a pointer to dicentric (9;20) in acute lymphoblastic leukemia
  Leukemia, 2000
• Clinical Significance of Deletions of Chromosome Arm 6q in Childhood Acute Lymphoblastic Leukemia: A Report from the Children's Cancer Group
  Leukemia & Lymphoma, 2000
• Combined spectral karyotyping and DAPI banding analysis of chromosome abnormalities in myelodysplastic syndrome
  Genes, Chromosomes and Cancer, 1999
• Incidence and Clinical Significance of CDKN2/MTS1/P16^ink4AND MTS2/P15^ink4BGene Deletions in Childhood Acute Lymphoblastic Leukemia
  Pediatric Hematology and Oncology, 1997
• Detection of the BCR-ABL gene by reverse transcription/polymerase chain reaction and fluorescence in situ hybridization in a patient with Philadelphia chromosome negative acute lymphoblastic leukaemia
  British Journal of Haematology, 1995
• dic(9; 20): A new recurrent chromosome abnormality in adult acute lymphoblastic leukemia
  Genes, Chromosomes and Cancer, 1995
• The detection of E2A rearrangement or E2A‐PBXI fusion transcript in t(1;19) leukemia to the editors
  Genes, Chromosomes and Cancer, 1995
• Variable breakpoints in Burkitt lymphoma cells with chromosomal t(8; 14) translocation separate c-myc and the IgH locus up to several hundred kb
  Human Molecular Genetics, 1992
• Extremely Poor Prognosis of Pediatric Acute Lymphoblastic Leukemia with Translocation (9;22): Updated Experience
  Leukemia & Lymphoma, 1992
• Prognostic implications of chromosomal findings in acute lymphoblastic leukaemia at diagnosis.
  BMJ, 1978