| 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 | ||
|
18.03.2022
12:14–12:16 |
P-CytoG-134 |
Unbalanced chromosome translocation between chromosomes Y and 17 as a rare cause of SHOX deficiency disorder |