| Zeit | ID | Programmpunkt | ||
|---|---|---|---|---|
|
18.03.2022 11:50–11:52 |
P-CancG-014 |
Germline variants in DNA repair genes including BRCA1/2 cause familial myeloproliferative neoplasms
Redezeit: 2 min in Session: Poster Session BasEpi / CancG / CytoG |
| Zeit | Titel der Session | |||
|---|---|---|---|---|
|
18.03.2022
14:00 – 15:30 |
Workshop 8
(Epi-)Genomics and Cancer |
| Zeit | ID | Programmpunkt | ||
|---|---|---|---|---|
|
16.03.2022
15:30–15:45 |
SEL-003 |
C2orf69 mutations disrupt mitochondrial function and cause a multisystem human disorder with recurring autoinflammation | ||
|
17.03.2022
15:00–15:02 |
P-ClinG-073 |
Genetic diagnostics in a MZEB – experiences of a pilot study | ||
|
17.03.2022
15:14–15:16 |
P-CancG-023 |
Tumor predisposition in young head and neck cancer patients | ||
|
17.03.2022
15:20–15:22 |
P-ClinG-093 |
Molecular diagnosis of ZFP57-associated 6q24 imprinting disturbances in a patient with suspected Beckwith-Wiedemann syndrome | ||
|
17.03.2022
15:20–15:22 |
P-MonoG-167 |
Novel variants broaden the mutational spectrum of Hereditary Sensory and Autonomic Neuropathy disorders | ||
|
18.03.2022
11:50–11:52 |
P-CancG-014 |
Germline variants in DNA repair genes including BRCA1/2 cause familial myeloproliferative neoplasms | ||
|
18.03.2022
12:08–12:10 |
P-ClinG-068 |
PHIP-associated Chung-Jansen syndrome: report of 14 new individuals |