Partial support for this essay came from the Postdoctoral fellowship program (Callier) of the Center for Genetic Research Ethics and Law, through the National Institutes of Health grant P50-HG003390 from the National Human Genome Research Institute. Harald Schmidt carried out this work while being supported by a Harkness Fellowship from the Commonwealth Fund. The views presented here are those of the author alone and should not be attributed to The Commonwealth Fund or its directors, officers, or staff or to CGREAL.
Managing Patient Expectations About Deidentification
Log in via your institution
Log in to Taylor & Francis Online
Restore content access
Restore content access for purchases made as guestPDF download + Online access
- 48 hours access to article PDF & online version
- Article PDF can be downloaded
- Article PDF can be printed
Issue Purchase
- 30 days online access to complete issue
- Article PDFs can be downloaded
- Article PDFs can be printed
Related Research
People also read lists articles that other readers of this article have read.
Recommended articles lists articles that we recommend and is powered by our AI driven recommendation engine.
Cited by lists all citing articles based on Crossref citations.
Articles with the Crossref icon will open in a new tab.