Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Equipe Genetique des Anomalies du Developpement, |
RCV001027687 | SCV001190257 | likely pathogenic | Cardiac anomalies - developmental delay - facial dysmorphism syndrome | 2019-05-10 | criteria provided, single submitter | clinical testing |