Importance of using comparative genomic hybridization to improve detection of chromosomal changes in childhood acute lymphoblastic leukemia
- 1 December 2000
- journal article
- research article
- Published by Elsevier in Cancer Genetics and Cytogenetics
- Vol. 123 (2) , 114-122
- https://doi.org/10.1016/s0165-4608(00)00310-1
Abstract
No abstract availableKeywords
This publication has 18 references indexed in Scilit:
- Comparative genomic hybridization in childhood acute lymphoblastic leukemiaLeukemia, 1998
- Comparative genomic hybridization as part of a new diagnostic strategy in childhood hyperdiploid acute lymphoblastic leukemiaLeukemia, 1998
- Comparative genomic hybridization is a powerful tool, complementary to cytogenetics, to identify chromosomal abnormalities in childhood acute lymphoblastic leukaemiaBritish Journal of Haematology, 1997
- Genetic aberrations in pediatric acute lymphoblastic leukemia by comparative genomic hybridizationCancer Genetics and Cytogenetics, 1997
- Childhood LeukemiasNew England Journal of Medicine, 1995
- Optimizing comparative genomic hybridization for analysis of DNA sequence copy number changes in solid tumorsGenes, Chromosomes and Cancer, 1994
- Biology and clinical significance of cytogenetic abnormalities in childhood acute lymphoblastic leukemiaBlood, 1990
- Chromosomal translocations play a unique role in influencing prognosis in childhood acute lymphoblastic leukemiaBlood, 1986
- Prognostic importance of chromosome number in 136 untreated children with acute lymphoblastic leukemiaBlood, 1982
- Prognostic implications of chromosomal findings in acute lymphoblastic leukaemia at diagnosis.BMJ, 1978