diepoxybutane has been researched along with Autosomal Chromosome Disorders in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (66.67) | 18.7374 |
| 1990's | 1 (33.33) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Alimena, G; Dallapiccola, B; Gandini, E; Mokini, V; Porfirio, B | 1 |
| Bungey, J; Dokal, I; Hows, J; Luzzatto, L; Oscier, D; Williamson, P | 1 |
| Auerbach, AD; Rogatko, A; Schroeder-Kurth, TM | 1 |
3 other study(ies) available for diepoxybutane and Autosomal Chromosome Disorders
| Article | Year |
|---|---|
Failure of diepoxybutane to enhance sister chromatid exchange levels in Fanconi's anemia patients and heterozygotes.
Topics: Adolescent; Adult; Anemia, Aplastic; Cells, Cultured; Chromosome Aberrations; Chromosome Disorders; Crossing Over, Genetic; Epoxy Compounds; Ethers, Cyclic; Fanconi Anemia; Female; Heterozygote; Humans; Lymphocytes; Male; Mutagens; Sister Chromatid Exchange | 1983 |
Dyskeratosis congenita fibroblasts are abnormal and have unbalanced chromosomal rearrangements.
Topics: Adolescent; Adult; Bone Marrow Diseases; Cell Survival; Cells, Cultured; Child; Chromosome Aberrations; Chromosome Disorders; Chromosome Mapping; Epoxy Compounds; Female; Fibroblasts; Gene Rearrangement; Genetic Linkage; Humans; Karyotyping; Male; Mutagens; Pedigree; Polymorphism, Restriction Fragment Length; Skin; X Chromosome | 1992 |
International Fanconi Anemia Registry: relation of clinical symptoms to diepoxybutane sensitivity.
Topics: Anemia, Aplastic; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human; DNA; Epoxy Compounds; Ethers, Cyclic; Fanconi Anemia; Female; Humans; International Cooperation; Male; Registries; Regression Analysis | 1989 |