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Analysis of VUS reporting, variant reinterpretation and recontact policies in clinical genomic sequencing consent forms
There are several key unsolved issues relating to the clinical use of next generation sequencing, such as: should laboratories report variants of uncertain significance (VUS) to clinicians and/or patients? Should they reinterpret VUS in response to growing knowledge in the field? And should patients...
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| Publicado no: | Eur J Hum Genet |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Springer International Publishing
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6244391/ https://ncbi.nlm.nih.gov/pubmed/30143804 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41431-018-0239-7 |
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