trolamine salicylate has been researched along with Chromosomal Translocation in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (50.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Aboura, A; Baumann, C; Benzacken, B; Boutaud, L; Capri, Y; Dupont, C; Guimiot, F; Le Du, N; Schaefer, E; Spaggiari, E; Tabet, AC | 1 |
| Boone, RA; Fitchett, M; Flint, J; Hilton-Jones, D; Horsley, SW; Huson, S; Kearney, L; Knight, SJ; Nixon, J | 1 |
2 other study(ies) available for trolamine salicylate and Chromosomal Translocation
| Article | Year |
|---|---|
COL2A1 gene disruption by a balanced translocation t(12;15)(q13;q22.2) in familial Stickler syndrome.
Topics: Adult; Arthritis; Child; Chromosome Banding; Chromosomes, Human, Pair 12; Chromosomes, Human, Pair 15; Collagen Type II; Comparative Genomic Hybridization; Connective Tissue Diseases; Female; Hearing Loss, Sensorineural; Humans; In Situ Hybridization, Fluorescence; Infant, Newborn; Male; Pregnancy; Retinal Detachment; Translocation, Genetic | 2013 |
Del(18p) shown to be a cryptic translocation using a multiprobe FISH assay for subtelomeric chromosome rearrangements.
Topics: Adult; Arthritis; Chromosome Aberrations; Chromosome Deletion; Chromosome Disorders; Chromosomes, Human, Pair 18; Female; Humans; In Situ Hybridization, Fluorescence; Karyotyping; Keratosis; Muscular Atrophy, Spinal; Telomere; Translocation, Genetic | 1998 |