cytosine has been researched along with Hamartoma Syndrome, Multiple in 1 studies
Hamartoma Syndrome, Multiple: A hereditary disease characterized by multiple ectodermal, mesodermal, and endodermal nevoid and neoplastic anomalies. Facial trichilemmomas and papillomatous papules of the oral mucosa are the most characteristic lesions. Individuals with this syndrome have a high risk of BREAST CANCER; THYROID CANCER; and ENDOMETRIAL CANCER. This syndrome is associated with mutations in the gene for PTEN PHOSPHATASE.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (100.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Koch, R | 1 |
| Scholz, M | 1 |
| Nelen, MR | 1 |
| Schwechheimer, K | 1 |
| Epplen, JT | 1 |
| Harders, AG | 1 |
1 review available for cytosine and Hamartoma Syndrome, Multiple
| Article | Year |
|---|---|
Lhermitte-Duclos disease as a component of Cowden's syndrome. Case report and review of the literature.
Topics: Cerebellar Neoplasms; Chromosomes, Human, Pair 10; Cytosine; Exons; Female; Ganglioneuroma; Genes, T | 1999 |