Sister chromatid exchanges, hyperdiploidy and chromosomal rearrangements studied in cells from melanoma-prone individuals belonging to families with the dysplastic nevus syndrome
- 1 January 1987
- journal article
- research article
- Published by Elsevier in Cancer Genetics and Cytogenetics
- Vol. 24 (1) , 33-43
- https://doi.org/10.1016/0165-4608(87)90081-1
Abstract
No abstract availableThis publication has 28 references indexed in Scilit:
- Acquired Precursors of Cutaneous Malignant MelanomaNew England Journal of Medicine, 1985
- Fragile sites and cancer breakpointsCancer Genetics and Cytogenetics, 1984
- Abnormal sensitivity to UV‐radiation in cultured skin ibroblasts from patients with hereditary cutaneous malignant melanoma and dysplastic nevus syndromeInternational Journal of Cancer, 1982
- Occurrence ofin vitro tetraploidy in the heritable colon cancer syndromesCancer, 1981
- Evidence of clonal attenuation, clonal succession, and clonal expansion in mass cultures of aging Werner’s syndrome skin fibroblastsCytogenetic and Genome Research, 1981
- Demonstration of a heritable fragile site in human chromosome 16 with distamycin ACytogenetic and Genome Research, 1980
- Familial atypical multiple mole-melanoma syndrome.Journal of Medical Genetics, 1978
- Specific chromosome aberrations in ataxia telangiectasia.Journal of Medical Genetics, 1975
- Variegated translocation mosaicism in human skin fibroblast culturesCytogenetic and Genome Research, 1975
- New Giemsa method for the differential staining of sister chromatidsNature, 1974