Two complementation groups of Fanconi's anemia differ in their phenotypic response to a DNA-crosslinking treatment
- 1 January 1987
- journal article
- research article
- Published by Springer Nature in Human Genetics
- Vol. 75 (1), 45-47
- https://doi.org/10.1007/bf00273837
Abstract
No abstract availableKeywords
This publication has 21 references indexed in Scilit:
- INHIBITION OF DNA SYNTHESIS BY PSORALEN‐INDUCED LESIONS IN XERODERMA PIGMENTOSUM AND FANCONI'S ANEMIA FIBROBLASTSPhotochemistry and Photobiology, 1985
- Clinical and cytogenetic diversity in Fanconi's anaemia.Journal of Medical Genetics, 1984
- Repair of Psoralen Adducts in Human DNA: Differences Among Xeroderma Pigmentosum Complementation GroupsJournal of Investigative Dermatology, 1984
- Genetically determined chromosome instability syndromesCytogenetic and Genome Research, 1982
- Specific cellular defects in patients with Fanconi anemiaJournal of Cellular Physiology, 1979
- DNA repair in a fanconi's anemia fibroblast cell strainBiochimica et Biophysica Acta (BBA) - Nucleic Acids and Protein Synthesis, 1979
- Cross-link repair in human cells and its possible defect in Fanconi's anemia cellsJournal of Molecular Biology, 1977
- Semi-conservative deoxyribonucleic acid synthesis in unirradiated and ultraviolet-irradiated xeroderma pigmentosum and normal human skin fibroblastsMutation Research, 1977
- Susceptibility of Fanconi's anaemia fibroblasts to chromosome damage by carcinogensNature, 1976
- Growth of cultured cells from patients with Fanconi anemiaJournal of Cellular Physiology, 1976