Systematic screening at diagnosis of −5/del(5)(q31), −7, or chromosome 8 aneuploidy by interphase fluorescence in situ hybridization in 110 acute myelocytic leukemia and high-risk myelodysplastic syndrome patients: concordances and discrepancies with conventional cytogenetics
- 1 July 2004
- journal article
- research article
- Published by Elsevier in Cancer Genetics and Cytogenetics
- Vol. 152 (1) , 29-41
- https://doi.org/10.1016/j.cancergencyto.2003.10.005
Abstract
No abstract availableKeywords
This publication has 45 references indexed in Scilit:
- Pretreatment cytogenetic abnormalities are predictive of induction success, cumulative incidence of relapse, and overall survival in adult patients with de novo acute myeloid leukemia: results from Cancer and Leukemia Group B (CALGB 8461)Blood, 2002
- The predictive value of hierarchical cytogenetic classification in older adults with acute myeloid leukemia (AML): analysis of 1065 patients entered into the United Kingdom Medical Research Council AML11 trialBlood, 2001
- Incidence, characterization and prognostic significance of chromosomal abnormalities in 640 patients with primary myelodysplastic syndromesBritish Journal of Haematology, 2000
- The Importance of Diagnostic Cytogenetics on Outcome in AML: Analysis of 1,612 Patients Entered Into the MRC AML 10 TrialBlood, 1998
- The significance of trisomy 8 in de novo acute myeloid leukaemia: the accompanying chromosome aberrations determine the prognosisBritish Journal of Haematology, 1997
- Diagnostic and Prognostic Significance of Cytogenetics in Adult Primary Myelodysplastic SyndromesLeukemia & Lymphoma, 1996
- Detection of monosomy 7 and trisomy 8 in myeloid neoplasia: a comparison of banding and fluorescence in situ hybridizationBlood, 1993
- Combination of classical and interphase cytogenetics to investigate the biology of myeloid disorders: Detection of masked monosomy 7 in AMLLeukemia Research, 1993
- Application of fluorescence in situ hybridization in hematological disordersCancer Genetics and Cytogenetics, 1992
- Detection of trisomy 8 in hematological disorders by in situ hybridizationCytogenetic and Genome Research, 1991