azacitidine has been researched along with Familial Turner Syndrome in 1 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 1 (100.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
De Moerloose, B; Decaluwe, W; Flotho, C; Hofmans, M; Lammens, T; Niemeyer, C; Philippé, J; Schröder, R; Van Roy, N | 1 |
1 other study(ies) available for azacitidine and Familial Turner Syndrome
Article | Year |
---|---|
Noonan syndrome-associated myeloproliferative disorder with somatically acquired monosomy 7: impact on clinical decision making.
Topics: Azacitidine; Chromosome Deletion; Chromosomes, Human, Pair 7; Clinical Decision-Making; DNA Methylation; Humans; Infant; Infant, Newborn; Male; Myeloproliferative Disorders; Noonan Syndrome | 2019 |