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Variation among Consent Forms for Clinical Whole Exome Sequencing
The goal of this study was to explore variation among informed consent documents for clinical whole exome sequencing (WES) in order to identify the level of consistency with the recommendations from the American College of Medical Genetics and Genomics (ACMG) and the Presidential Commission for the...
Tallennettuna:
| Julkaisussa: | J Genet Couns |
|---|---|
| Päätekijät: | , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Springer US
2017
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5794809/ https://ncbi.nlm.nih.gov/pubmed/28689263 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10897-017-0127-2 |
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