cytosine has been researched along with Genetic Diseases, X-Chromosome Linked in 5 studies
| 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 | 3 (60.00) | 29.6817 |
| 2010's | 1 (20.00) | 24.3611 |
| 2020's | 1 (20.00) | 2.80 |
| Authors | Studies |
|---|---|
| Alhamoudi, KM | 1 |
| Alghamdi, B | 1 |
| Alswailem, M | 1 |
| Nasir, A | 1 |
| Aljomaiah, A | 1 |
| Al-Hindi, H | 1 |
| Alzahrani, AS | 1 |
| Wolfswinkel, EM | 1 |
| Weathers, WM | 1 |
| Correa, B | 1 |
| Buchanan, EP | 1 |
| Hollier, LH | 1 |
| Kim, JW | 1 |
| Simmer, JP | 1 |
| Hu, YY | 1 |
| Lin, BP | 1 |
| Boyd, C | 1 |
| Wright, JT | 1 |
| Yamada, CJ | 1 |
| Rayes, SK | 1 |
| Feigal, RJ | 1 |
| Hu, JC | 1 |
| Kida, M | 1 |
| Sakiyama, Y | 1 |
| Matsuda, A | 1 |
| Takabayashi, S | 1 |
| Ochi, H | 1 |
| Sekiguchi, H | 1 |
| Minamitake, S | 1 |
| Ariga, T | 1 |
| Zhang, B | 1 |
| Liu, Z | 1 |
| Zhao, G | 1 |
| Xie, X | 1 |
| Yin, X | 1 |
| Hu, Z | 1 |
| Xu, S | 1 |
| Li, Q | 1 |
| Song, F | 1 |
| Tian, J | 1 |
| Luo, W | 1 |
| Ding, M | 1 |
| Yin, J | 1 |
| Xia, K | 1 |
| Xia, J | 1 |
5 other studies available for cytosine and Genetic Diseases, X-Chromosome Linked
| Article | Year |
|---|---|
A Unique Mechanism of a Novel Synonymous PHEX Variant Causing X-Linked Hypophosphatemia.
Topics: Adenine; Amino Acids; Codon, Terminator; Cytosine; DNA, Complementary; Familial Hypophosphatemic Ric | 2022 |
Craniofrontonasal dysplasia: variability of the frontonasal suture and implications for treatment.
Topics: Child; Codon; Cranial Sutures; Craniofacial Abnormalities; Craniosynostoses; Cytosine; Ephrin-B1; Fe | 2013 |
Amelogenin p.M1T and p.W4S mutations underlying hypoplastic X-linked amelogenesis imperfecta.
Topics: Amelogenesis Imperfecta; Amelogenin; Child; Codon; Cytosine; Dental Enamel; Dental Enamel Hypoplasia | 2004 |
A novel missense mutation (p.P52R) in amelogenin gene causing X-linked amelogenesis imperfecta.
Topics: Amelogenesis Imperfecta; Amelogenin; Arginine; Cytosine; Dental Enamel; Exons; Female; Genetic Disea | 2007 |
Novel mutations of the FRMD7 gene in X-linked congenital motor nystagmus.
Topics: Asian People; Codon, Nonsense; Cytosine; Cytoskeletal Proteins; Female; Genetic Diseases, X-Linked; | 2007 |