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A missing link in the bench-to-bedside paradigm: engaging regulatory stakeholders in clinical genomics research
For genomic medicine research to be fully translated into clinical care, it is critical for researchers to engage stakeholders who ultimately regulate the use of genomic technologies and therapeutics within healthcare practice. Herein, we describe an example of how this might work.
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2016
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5031300/ https://www.ncbi.nlm.nih.gov/pubmed/27655359 http://dx.doi.org/10.1186/s13073-016-0351-7 |