Chromosome breakage in Fanconi's anemia and normal cells following in vitro and in vivo cocultivation
- 1 December 1986
- journal article
- research article
- Published by Elsevier in Cancer Genetics and Cytogenetics
- Vol. 23 (4) , 315-320
- https://doi.org/10.1016/0165-4608(86)90014-2
Abstract
No abstract availableThis publication has 19 references indexed in Scilit:
- Further characterization of the ataxia-telangiectasia clastogenic factor by reversed-phase liquid chromatographyJournal of Biotechnology, 1984
- Fanconi's anemia: A cytogenetic study on lymphocyte and bone marrow cultures utilizing 1,2:3,4-diepoxybutaneCancer Genetics and Cytogenetics, 1983
- Prenatal diagnosis of ataxia telangiectasiaThe Journal of Pediatrics, 1982
- Prevention of chromosomal breakage in Fanconi's anemia by cocultivation with normal cellsHuman Genetics, 1980
- Bone Marrow Transplantation in Fanconi AnaemiaBritish Journal of Haematology, 1980
- Sister chromatid exchange in cells metabolically coupled to Bloom's syndrome cellsNature, 1980
- A diffusable clastogenic factor in ataxia telangiectasiaCytogenetic and Genome Research, 1980
- Effect of cocultivation on sister chromatid exchange frequencies in Bloom's syndrome and normal fibroblast cellsNature, 1978
- Susceptibility of Fanconi's anaemia fibroblasts to chromosome damage by carcinogensNature, 1976
- Ataxia telangiectasia: a human mutation with abnormal radiation sensitivityNature, 1975