| Zeit | ID | Programmpunkt | ||
|---|---|---|---|---|
|
18.03.2022 11:52–11:54 |
P-ClinG-052 |
Towards European Standard Clinical Practice guidance for individuals with familial leukemia
Redezeit: 2 min in Session: Poster Session ClinG 2 |
| Zeit | ID | Programmpunkt | ||
|---|---|---|---|---|
|
17.03.2022
15:22–15:24 |
P-Techno-195 |
GenOtoScope: Automated annotation of variants associated with hereditary hearing loss | ||
|
17.03.2022
17:15–17:30 |
W4-006 |
Rare germline variants in the E-cadherin gene CDH1 are associated with an increased risk of brain tumors of neuroepithelial and epithelial origin | ||
|
18.03.2022
11:52–11:54 |
P-ClinG-052 |
Towards European Standard Clinical Practice guidance for individuals with familial leukemia | ||
|
18.03.2022
12:06–12:08 |
P-CancG-032 |
Rare germline variants in the POLE and POLD1 genes in familial glioma |