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Consent for clinical genome sequencing: considerations from the Clinical Sequencing Exploratory Research Consortium
Implementing genome and exome sequencing in clinical practice presents challenges, including obtaining meaningful informed consent. Consent may be challenging due to test limitations such as uncertainties associated with test results and interpretation, complexity created by the potential for additi...
Guardat en:
| Publicat a: | Per Med |
|---|---|
| Autors principals: | , , , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Future Medicine Ltd
2019
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6681646/ https://ncbi.nlm.nih.gov/pubmed/31313633 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2217/pme-2018-0076 |
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