cytosine has been researched along with Hypertelorism in 2 studies
Hypertelorism: Abnormal increase in the interorbital distance due to overdevelopment of the lesser wings of the sphenoid.
| Excerpt | Relevance | Reference |
|---|---|---|
| "In place of the typical craniosynostosis found in CFND, she presented with a superiorly displaced nasion and an anomalously positioned frontonasal suture." | 1.39 | Craniofrontonasal dysplasia: variability of the frontonasal suture and implications for treatment. ( Buchanan, EP; Correa, B; Hollier, LH; Weathers, WM; Wolfswinkel, EM, 2013) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (50.00) | 29.6817 |
| 2010's | 1 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Wolfswinkel, EM | 1 |
| Weathers, WM | 1 |
| Correa, B | 1 |
| Buchanan, EP | 1 |
| Hollier, LH | 1 |
| Kosaki, K | 1 |
| Ogata, T | 1 |
| Kosaki, R | 1 |
| Sato, S | 1 |
| Matsuo, N | 1 |
2 other studies available for cytosine and Hypertelorism
| Article | Year |
|---|---|
Craniofrontonasal dysplasia: variability of the frontonasal suture and implications for treatment.
Topics: Child; Codon; Cranial Sutures; Craniofacial Abnormalities; Craniosynostoses; Cytosine; Ephrin-B1; Fe | 2013 |
A novel mutation in the FOXL2 gene in a patient with blepharophimosis syndrome: differential role of the polyalanine tract in the development of the ovary and the eyelid.
Topics: Blepharophimosis; Blepharoptosis; Child; Cytosine; DNA Mutational Analysis; DNA Primers; DNA-Binding | 2002 |