thymine has been researched along with Genetic Diseases, Inborn in 1 studies
Genetic Diseases, Inborn: Diseases that are caused by genetic mutations present during embryo or fetal development, although they may be observed later in life. The mutations may be inherited from a parent's genome or they may be acquired in utero.
| 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 |
|---|---|
| Chastain, PD | 1 |
| Sinden, RR | 1 |
1 review available for thymine and Genetic Diseases, Inborn
| Article | Year |
|---|---|
CTG repeats associated with human genetic disease are inherently flexible.
Topics: Cytosine; Genetic Diseases, Inborn; Guanine; Humans; Nervous System Diseases; Nucleic Acid Conformat | 1998 |