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A deliberative study of public attitudes towards sharing genomic data within NHS genomic medicine services in England
Whole genome (DNA) sequencing is becoming part of routine care healthcare in England. Genomic data are most useful when pooled with other patients’ data, meaning that clinicians may need to share data to effectively treat patients. We ran deliberative focus groups to explore views among 44 patients...
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| Udgivet i: | Public Underst Sci |
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| Main Authors: | , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
SAGE Publications
2020
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7539600/ https://ncbi.nlm.nih.gov/pubmed/32664786 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/0963662520942132 |
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