nsc-172755 has been researched along with Elliptocytosis, Hereditary in 1 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (100.00) | 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 |
|---|---|
| Bournier, O; Devaux, I; Dhermy, D; Forget, BG; Galand, C; Gallagher, PG; Garbarz, M; Gautero, H; Glele-Kakai, C; Leborgne, S; Lecomte, MC; Zohoun, I | 1 |
1 other study(ies) available for nsc-172755 and Elliptocytosis, Hereditary
| Article | Year |
|---|---|
Epidemiological studies of spectrin mutations related to hereditary elliptocytosis and spectrin polymorphisms in Benin.
Topics: Benin; Elliptocytosis, Hereditary; Genetic Testing; Humans; Mutation; Point Mutation; Polymerase Chain Reaction; Polymorphism, Genetic; Spectrin | 1996 |