Chromosome 22q11.2 Deletion Syndrome
2 clinical trials · Condition
◉ Watch Chromosome 22q11.2 Deletion Syndrome
| Record | Firm | Date |
|---|---|---|
| Parent and Infant Inter(X)Action Intervention (PIXI) (NCT03836300) | RTI International | 2018-11-30 |
| Genetics and Psychopathology in the 22q11 Deletion Syndrome (NCT00161109) | UMC Utrecht | 2002-10-01 |
Track Chromosome 22q11.2 Deletion Syndrome automatically
Every clearance here is in the API, with alerts when new ones post.