Recessive mutations and chromosome deletions leading to cancer
- 1 April 1989
- journal article
- review article
- Published by Oxford University Press (OUP) in British Journal of Surgery
- Vol. 76 (4), 327-330
- https://doi.org/10.1002/bjs.1800760404
Abstract
This review examines the effect that a small chromosome deletion affecting a specific DNA sequence may have in producing a state of ‘hemizygosity’ for a gene or genes, and so triggering malignancy of the cells concerned. The association between such deletions and a variety of cancers will be considered and the implications for clinical practice will be outlined.Keywords
Funding Information
- Spastics Society and the Paget Foundation
This publication has 36 references indexed in Scilit:
- The Molecular Genetics of CancerScience, 1987
- Retinoblastoma and Cancer GeneticsNew England Journal of Medicine, 1986
- Molecular Genetics of Human B- and T-cell NeoplasiaCold Spring Harbor Symposia on Quantitative Biology, 1986
- The Action of Oncogenes in the Cytoplasm and NucleusScience, 1985
- The Chromosomal Basis of Human NeoplasiaScience, 1983
- Human c-myc onc gene is located on the region of chromosome 8 that is translocated in Burkitt lymphoma cells.Proceedings of the National Academy of Sciences, 1982
- Chromosome Abnormalities in Malignant Hematologic DiseasesAdvances in Cancer Research, 1982
- The Origin and Development of Human Tumors Studied with Cell MarkersNew England Journal of Medicine, 1974
- A New Consistent Chromosomal Abnormality in Chronic Myelogenous Leukaemia identified by Quinacrine Fluorescence and Giemsa StainingNature, 1973
- Zytologische Untersuchungen über die Natur maligner TumorenCell and tissue research, 1930