Molecular features of primary MDS with cytogenetic changes
- 1 April 1998
- journal article
- review article
- Published by Elsevier in Leukemia Research
- Vol. 22 (4) , 293-302
- https://doi.org/10.1016/s0145-2126(97)00193-8
Abstract
No abstract availableKeywords
This publication has 62 references indexed in Scilit:
- Defining tumour-suppressor genesNature, 1997
- Mosaicism of the 5q deletion as assessed by interphase FISH is a common phenomenon in MDS and restricted to myeloid cellsLeukemia, 1997
- The 5q-syndromeBlood, 1994
- Consistent loss of the D5S89 locus mapping telomeric to the interleukin gene cluster and centromeric to EGR-1 in patients with 5q- chromosomeBlood, 1994
- Somatic mutations in the neurofibromatosis 1 gene in human tumorsCell, 1992
- Possible evidence for genomic imprinting in childhood acute myeloblastic leukaemia associated with monosomy for chromosome 7British Journal of Haematology, 1992
- Recommendations for a morphologic, immunologic, and cytogenetic (MIC) working classification of the primary and therapy-related myelodysplastic disordersCancer Genetics and Cytogenetics, 1988
- Morphologic, immunologic, and cytogenetic (MIC) working classification of the acute myeloid leukemias: Report of the workshop held in Leuven, Belgium, September 15–17, 1986Cancer Genetics and Cytogenetics, 1988
- The 5q− anomalyCancer Genetics and Cytogenetics, 1985
- Distinct haematological disorder with deletion of long arm of No. 5 chromosomeNature, 1974