clinical trial | Q30612 |
P3098 | ClinicalTrials.gov ID | NCT00556530 |
P17 | country | United States of America | Q30 |
P582 | end time | 2020-07-01 | |
P1050 | medical condition | syndrome | Q179630 |
Marfan syndrome | Q208562 | ||
DiGeorge syndrome | Q525642 | ||
P1132 | number of participants | 1000 | |
P6153 | research site | Children's Hospital of Philadelphia | Q4569202 |
P580 | start time | 2016-07-01 | |
P8363 | study type | observational study | Q818574 |
P1476 | title | Genetic Modifiers of 22q11.2 Deletion Syndrome |
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