| Zeit | ID | Programmpunkt | ||
|---|---|---|---|---|
|
17.03.2022
15:14–15:16 |
P-ClinG-087 |
Prenatal phenotype of PNKP-related primary microcephaly and unexpected complex variant mechanisms in RNA-analysis | ||
|
18.03.2022
12:06–12:08 |
P-ClinG-066 |
Novel OTUD5 variant detected in a patient with multiple congenital anomalies-neurodevelopmental syndrome and suggested in a fetus in the same family |