Found: 2
Select item for more details and to access through your institution.
Developing an online, searchable database to systematically map and organise current literature on retention research (ORRCA2).
- Published in:
- Clinical Trials, 2022, v. 19, n. 1, p. 71, doi. 10.1177/17407745211053803
- By:
- Publication type:
- Article
Inherited MUTYH mutations cause elevated somatic mutation rates and distinctive mutational signatures in normal human cells.
- Published in:
- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-31341-0
- By:
- Publication type:
- Article