The detection of trisomies 8 and 9 in patients with essential thrombocytosis by fluorescence in situ hybridization
- 30 November 1996
- journal article
- Published by Elsevier in Cancer Genetics and Cytogenetics
- Vol. 92 (1) , 14-17
- https://doi.org/10.1016/s0165-4608(96)00115-x
Abstract
No abstract availableKeywords
This publication has 22 references indexed in Scilit:
- Detection of trisomy 8 in hematological disorders by in situ hybridizationCytogenetic and Genome Research, 1991
- Cytogenetic analysis in essential thrombocythemia at diagnosis and at transformation: A 12-year studyCancer Genetics and Cytogenetics, 1989
- Three‐color fluorescence in situ hybridization for the simultaneous detection of multiple nucleic acid sequencesCytometry, 1989
- The preleukemic syndrome (hematopoietic dysplasia)Blood Reviews, 1988
- Cytogenetics of acutely transformed chronic myeloproliferative syndromes without a Philadelphia chromosome: A multicenter study of 55 patientsCancer Genetics and Cytogenetics, 1988
- A chromosomal profile of polycythemia veraCancer Genetics and Cytogenetics, 1987
- Chromosome Abnormalities in MyelofibrosisActa Haematologica, 1987
- Absence of a specific chromosomal marker in essential thrombocythemiaCancer Genetics and Cytogenetics, 1984
- Correlation of a specific chromosomal marker, 21q-, and retroviral indicators in patients with thrombocythemiaCancer Letters, 1979
- Chromosome Studies in Untreated Polycythaemia VeraScandinavian Journal of Haematology, 1976