cytosine has been researched along with Bessel-Hagen Disease in 1 studies
Excerpt | Relevance | Reference |
---|---|---|
"Hereditary multiple exostosis (HME) is an autosomal dominant disorder characterized by the development of benign cartilage-capped tumors at the juxta-epiphyseal regions of long bones." | 1.33 | A novel EXT1 splice site mutation in a kindred with hereditary multiple exostosis and osteoporosis. ( Christie, PT; Eastell, R; Harding, B; Javor, T; Kotanko, P; Lemos, MC; Smith, C; Thakker, RV, 2005) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (100.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Lemos, MC | 1 |
Kotanko, P | 1 |
Christie, PT | 1 |
Harding, B | 1 |
Javor, T | 1 |
Smith, C | 1 |
Eastell, R | 1 |
Thakker, RV | 1 |
1 other study available for cytosine and Bessel-Hagen Disease
Article | Year |
---|---|
A novel EXT1 splice site mutation in a kindred with hereditary multiple exostosis and osteoporosis.
Topics: Adolescent; Adult; Bone Density; Case-Control Studies; Cytosine; DNA, Recombinant; Exostoses, Multip | 2005 |