thymine has been researched along with Craniofacial Abnormalities in 2 studies
Craniofacial Abnormalities: Congenital structural deformities, malformations, or other abnormalities of the cranium and facial bones.
| 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 |
| Meyer-Marcotty, P | 1 |
| Weisschuh, N | 1 |
| Dressler, P | 1 |
| Hartmann, J | 1 |
| Stellzig-Eisenhauer, A | 1 |
2 other studies available for thymine and Craniofacial Abnormalities
| 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 |
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 |