| Zeit | ID | Programmpunkt | ||
|---|---|---|---|---|
|
18.03.2022 11:40–11:42 |
P-ClinG-034 |
First description of inheritance of a postzygotic OPA1 mosaic variant
Redezeit: 2 min in Session: Poster Session ClinG 2 |
| Zeit | ID | Programmpunkt | ||
|---|---|---|---|---|
|
17.03.2022
15:20–15:22 |
P-ClinG-065 |
NSDHL mutation as a rare cause of fetal cortical malformation | ||
|
18.03.2022
11:40–11:42 |
P-ClinG-034 |
First description of inheritance of a postzygotic OPA1 mosaic variant | ||
|
18.03.2022
12:08–12:10 |
P-ClinG-104 |
9p Deletion 9p24.3p23 in an 8-year old Girl with Developmental Delay, a large Head Circumference and Brachydactyly |