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Obtaining informed consent for clinical tumor and germline exome sequencing of newly diagnosed childhood cancer patients
BACKGROUND: Effectively educating families about the risks and benefits of genomic tests such as whole exome sequencing (WES) offers numerous challenges, including the complexity of test results and potential loss of privacy. Research on best practices for obtaining informed consent (IC) in a variet...
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| 主要な著者: | , , , , , , , , , , , , , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
BioMed Central
2014
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| 主題: | |
| オンライン・アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4195891/ https://ncbi.nlm.nih.gov/pubmed/25317207 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13073-014-0069-3 |
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