Correlation of N-ras point mutations with specific chromosomal abnormalities in primary myelodysplastic syndrome
- 28 February 1998
- journal article
- Published by Elsevier in Leukemia Research
- Vol. 22 (2) , 125-134
- https://doi.org/10.1016/s0145-2126(97)00112-4
Abstract
No abstract availableKeywords
This publication has 22 references indexed in Scilit:
- Hematologic, clinical, and cytogenetic analysis in 109 patients with primary myelodysplastic syndrome: Prognostic significance of morphology and chromosome findingsCancer Genetics and Cytogenetics, 1994
- Genetic lesions and clinical outcome in myelodysplasia (MDS)Leukemia Research, 1994
- MyelodysplasiaCurrent Opinion in Oncology, 1994
- The effector interactions of p21rasTrends in Biochemical Sciences, 1993
- N-ras mutations are associated with poor prognosis and increased risk of leukemia in myelodysplastic syndromeBlood, 1993
- Karyotypic analysis in primary myelodysplastic syndromesBlood Reviews, 1993
- Regulation of p21ras activityTrends in Genetics, 1991
- Analysis of N-RAS exon-1 mutations in myelodysplastic syndromes by polymerase chain reaction and direct sequencingBlood, 1989
- Prognostic implications of morphology and karyotype in primary myelodysplastic syndromesBlood, 1986
- Proposals for the classification of the myelodysplastic syndromesBritish Journal of Haematology, 1982