Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Institute of Human Genetics, |
RCV003126404 | SCV003803097 | uncertain significance | Noonan syndrome 1 | 2000-12-29 | criteria provided, single submitter | clinical testing | IrgendeinKommentar |