adenine has been researched along with Familial Turner Syndrome in 1 studies
| Excerpt | Relevance | Reference |
|---|---|---|
| "Noonan syndrome is a well-known clinical entity comprising multiple congenital anomalies characterized by typical facial features, short stature and congenital heart defect." | 1.32 | Genetics and variation in phenotype in Noonan syndrome. ( Jongmans, M; Noordam, K; Otten, B; van der Burgt, I, 2004) |
| 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 |
|---|---|
| Jongmans, M | 1 |
| Otten, B | 1 |
| Noordam, K | 1 |
| van der Burgt, I | 1 |
1 other study available for adenine and Familial Turner Syndrome
| Article | Year |
|---|---|
Genetics and variation in phenotype in Noonan syndrome.
Topics: Adenine; Adult; Child; Cytosine; Exons; Female; Genetic Variation; Genotype; Guanine; Humans; Infant | 2004 |