cytosine 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 |
---|---|
Sale, MM | 1 |
Craig, JE | 1 |
Charlesworth, JC | 1 |
FitzGerald, LM | 1 |
Hanson, IM | 1 |
Dickinson, JL | 1 |
Matthews, SJ | 1 |
Heyningen Vv, Vv | 1 |
Fingert, JH | 1 |
Mackey, DA | 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 cytosine and Aniridia
Article | Year |
---|---|
Broad phenotypic variability in a single pedigree with a novel 1410delC mutation in the PST domain of the PAX6 gene.
Topics: Aniridia; Cytosine; DNA Mutational Analysis; Eye Proteins; Female; Genetic Variation; Homeodomain Pr | 2002 |
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 |