adenine has been researched along with Basal Cell Nevus Syndrome in 2 studies
Basal Cell Nevus Syndrome: Hereditary disorder consisting of multiple basal cell carcinomas, odontogenic keratocysts, and multiple skeletal defects, e.g., frontal and temporoparietal bossing, bifurcated and splayed ribs, kyphoscoliosis, fusion of vertebrae, and cervicothoracic spina bifida. Genetic transmission is autosomal dominant.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Cleft palate is found in 4% of individuals with nevoid basal cell carcinoma syndrome." | 1.33 | Contributions of PTCH gene variants to isolated cleft lip and palate. ( Castilla, EE; Cooper, ME; Goldstein, T; Lopez Camelo, JS; Mansilla, MA; Marazita, ML; Murray, JC, 2006) |
| 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 |
|---|---|
| Wang, W | 1 |
| Wang, J | 1 |
| Li, J | 1 |
| Mao, L | 1 |
| Guo, F | 1 |
| Zhang, B | 1 |
| Mansilla, MA | 1 |
| Cooper, ME | 1 |
| Goldstein, T | 1 |
| Castilla, EE | 1 |
| Lopez Camelo, JS | 1 |
| Marazita, ML | 1 |
| Murray, JC | 1 |
2 other studies available for adenine and Basal Cell Nevus Syndrome
| Article | Year |
|---|---|
New mutation of the patched homologue 1 gene in a Chinese family with naevoid basal cell carcinoma syndrome.
Topics: Adenine; Basal Cell Nevus Syndrome; Chromosomes, Human, Pair 9; Codon, Nonsense; Cytosine; Exons; Hu | 2009 |
Contributions of PTCH gene variants to isolated cleft lip and palate.
Topics: Adenine; Alleles; Basal Cell Nevus Syndrome; Case-Control Studies; Cleft Lip; Cleft Palate; Cytosine | 2006 |