Informed consent for whole-genome sequencing studies in the clinical setting. Proposed recommendations on essential content and process
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Title
Informed consent for whole-genome sequencing studies in the clinical setting. Proposed recommendations on essential content and process
Authors
Keywords
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Journal
EUROPEAN JOURNAL OF HUMAN GENETICS
Volume 21, Issue 10, Pages 1054-1059
Publisher
Springer Nature America, Inc
Online
2013-01-16
DOI
10.1038/ejhg.2012.297
References
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Note: Only part of the references are listed.- The role of disease characteristics in the ethical debate on personal genome testing
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- Use of Whole-Genome Sequencing to Diagnose a Cryptic Fusion Oncogene
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- Ensuring the Safe Use of Genomic Medicine in Children
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- Personal genomics: information can be harmful
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- Whole Genome Scanning: Resolving Clinical Diagnosis and Management Amidst Complex Data
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