HIGHLIGHTS
- who: Posted Date April et al. from the University of Toronto have published the paper: A comprehensive genomic reporting structure for communicating all clinically signiufffdcant primary and secondary ufffdndings, in the Journal: (JOURNAL)
- what: The aim of this study was to develop a comprehensive genomic test report with accompanying consultation letters for patients and providers to promote the effective communication of all clinically-significant sequence variants (including single nucleotide variants (SNVs) and small insertions and deletions) resulting from GS. Categories of SFs reported in the trial are not typically analyzed or reported by clinical labs . . .
If you want to have access to all the content you need to log in!
Thanks :)
If you don't have an account, you can create one here.