Characterization of 20q deletions in patients with myeloproliferative disorders or myelodysplastic syndromes
- 1 April 1995
- journal article
- Published by Elsevier in Cancer Genetics and Cytogenetics
- Vol. 80 (2) , 87-94
- https://doi.org/10.1016/0165-4608(94)00150-a
Abstract
No abstract availableKeywords
This publication has 36 references indexed in Scilit:
- De novo myelodysplastic syndrome (MDS) with deletion of the long arm of chromosome 20: A subtype of MDS with distinct hematological and prognostic features?Leukemia Research, 1993
- Clinical significance of the del(20q) chromosome in hematologic disordersCancer Genetics and Cytogenetics, 1992
- Chromosomal deletions in the myelodysplastic syndromeLeukemia Research, 1992
- Localization of the SRC oncogene to chromosome band 20q11.2 and loss of this gene with deletion (20q) in two leukemic patientsBlood, 1989
- Cytogenetic studies and their prognostic significance in agnogenic myeloid metaplasia: a report on 47 casesBlood, 1988
- A chromosomal profile of polycythemia veraCancer Genetics and Cytogenetics, 1987
- Chromosome studies in polycythemia vera patientsCancer Genetics and Cytogenetics, 1984
- Hematologic manifestations associated with deletions of the long arm of chromosome 20Cancer Genetics and Cytogenetics, 1984
- Identity of the abnormal F-group chromosome associated with polycythaemia veraPublished by Springer Nature ,1972
- The Chromosomes in Polycythaemia VeraBritish Journal of Haematology, 1966