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From the Data on Many, Precision Medicine for “One”: The Case for Widespread Genomic Data Sharing
Within the decade, genome sequencing promises to become a routine part of healthcare around the globe. Many millions of genomes linked to health records will soon be available for researchers and clinicians to make use of to advance precision medicine. To realise the full impact of genomic medicine,...
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| Publicat a: | Biomed Hub |
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| Autors principals: | , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
S. Karger AG
2017
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6945905/ https://ncbi.nlm.nih.gov/pubmed/31988941 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000481682 |
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