bromodeoxyuridine has been researched along with Genetic Diseases, Inborn in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (33.33) | 18.7374 |
| 1990's | 2 (66.67) | 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 |
|---|---|
| Dougherty, CP; Latt, SA; Loveday, KS; Schreck, RR; Shuler, CF | 1 |
| Knuutila, S; Larramendy, M | 1 |
| Back, E; Schempp, W; Voiculescu, I | 1 |
1 review(s) available for bromodeoxyuridine and Genetic Diseases, Inborn
| Article | Year |
|---|---|
Sister chromatid exchanges.
Topics: Animals; Bromodeoxyuridine; Carcinogens; Chromosomes; Cricetinae; Crossing Over, Genetic; Cyclophosphamide; Cytological Techniques; Deer; Dipodomys; DNA; DNA Repair; DNA Replication; Dose-Response Relationship, Drug; Drosophila melanogaster; Female; Fluorescent Dyes; Genetic Diseases, Inborn; Humans; Karyotyping; Male; Meiosis; Mice; Mitomycins; Mutagens; Rats; Sister Chromatid Exchange; Spermatogonia; Staining and Labeling | 1980 |
2 other study(ies) available for bromodeoxyuridine and Genetic Diseases, Inborn
| Article | Year |
|---|---|
Sister chromatid differentiation and chromosomal in situ suppression hybridization: a combined methodology for analyzing cell proliferation and SCEs in individual chromosomes.
Topics: Bromodeoxyuridine; Cell Division; Cells, Cultured; Chromosomes, Human, Pair 12; Fibroblasts; Genetic Diseases, Inborn; Humans; In Situ Hybridization; Kinetics; Metaphase; Mitosis; Mosaicism; Sister Chromatid Exchange; Syndrome | 1992 |
Homozygous condition for a BrdU-requiring fragile site on chromosome 12.
Topics: Bromodeoxyuridine; Cells, Cultured; Chromosome Fragile Sites; Chromosome Fragility; Chromosomes, Human, Pair 12; Genetic Diseases, Inborn; Homozygote; Humans; Lymphocytes; Metaphase | 1991 |