| Zeit | ID | Programmpunkt | ||
|---|---|---|---|---|
|
17.03.2022
15:08–15:10 |
P-ClinG-081 |
Identification of a novel pathogenic TCNT3 variant in a 46,XY fetus with Meckel-Gruber syndrome and sex reversal | ||
|
18.03.2022
11:44–11:46 |
P-ClinG-044 |
Poirier-Bienvenu neurodevelopmental syndrome in three brothers due to a pathogenic CSNK2B-variant and paternal germ line mosaicism |