cytosine has been researched along with Eye Abnormalities in 4 studies
Eye Abnormalities: Congenital absence of or defects in structures of the eye; may also be hereditary.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 4 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Brooks, BP | 1 |
| Dagenais, SL | 1 |
| Nelson, CC | 1 |
| Glynn, MW | 1 |
| Caulder, MS | 1 |
| Downs, CA | 1 |
| Glover, TW | 1 |
| Vanita, V | 1 |
| Singh, JR | 1 |
| Hejtmancik, JF | 1 |
| Nuernberg, P | 1 |
| Hennies, HC | 1 |
| Singh, D | 1 |
| Sperling, K | 1 |
| Wang, J | 1 |
| Liu, J | 1 |
| Zhang, Q | 1 |
| Meyer-Marcotty, P | 1 |
| Weisschuh, N | 1 |
| Dressler, P | 1 |
| Hartmann, J | 1 |
| Stellzig-Eisenhauer, A | 1 |
4 other studies available for cytosine and Eye Abnormalities
| Article | Year |
|---|---|
Mutation of the FOXC2 gene in familial distichiasis.
Topics: Adenine; Adolescent; Adult; Base Sequence; Codon; Cytosine; DNA Mutational Analysis; DNA-Binding Pro | 2003 |
A novel fan-shaped cataract-microcornea syndrome caused by a mutation of CRYAA in an Indian family.
Topics: Asian People; Base Sequence; Cataract; Child; Chromosome Mapping; Chromosomes, Human, Pair 21; Corne | 2006 |
FOXL2 mutations in Chinese patients with blepharophimosis-ptosis-epicanthus inversus syndrome.
Topics: Asian People; Blepharophimosis; Blepharoptosis; Cysteine; Cytosine; Eye Abnormalities; Eyelids; Fork | 2007 |
Morphology of the sella turcica in Axenfeld-Rieger syndrome with PITX2 mutation.
Topics: Adolescent; Cephalometry; Chromosomes, Human, Pair 13; Codon; Cranial Fossa, Posterior; Craniofacial | 2008 |