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 |