thymine has been researched along with Aniridia in 2 studies
Aniridia: A congenital abnormality in which there is only a rudimentary iris. This is due to the failure of the optic cup to grow. Aniridia also occurs in a hereditary form, usually autosomal dominant.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| De Becker, I | 1 |
| Walter, M | 1 |
| Noël, LP | 1 |
| Neethirajan, G | 1 |
| Nallathambi, J | 1 |
| Krishnadas, SR | 1 |
| Vijayalakshmi, P | 1 |
| Shashikanth, S | 1 |
| Collinson, JM | 1 |
| Sundaresan, P | 1 |
2 other studies available for thymine and Aniridia
| Article | Year |
|---|---|
Phenotypic variations in patients with a 1630 A>T point mutation in the PAX6 gene.
Topics: Adenine; Adult; Aniridia; Cataract; Child, Preschool; Corneal Diseases; Eye Proteins; Female; Geneti | 2004 |
Identification of novel mutant PAX6 alleles in Indian cases of familial aniridia.
Topics: Alleles; Aniridia; Asian People; Codon, Nonsense; Cytosine; DNA Transposable Elements; Exons; Eye Pr | 2006 |