Document Type
Survey
Title

Genomic Information and the Right Not to Know Questionnaire

Author(s):

Author Name(s)
Flatau, L.
Reitt, M.
Duttge, G.
Lenk, C.
Zoll, B.
Poser, W.
Weber, A.
Heilbronner, U.
Rietschel, M.
Strohmaier, J.
Kesberg, R.
Nagel, J.
& Schulze, T. G.

Year:

Year
2018

Flatau and colleagues developed this survey to assess informational preferences among German patients, healthcare professionals, and members of the public in a genetic testing context. The survey assesses participant characteristics, preferences about the return of genetic results, attitudes about physician disclosure, and willingness to share test results.

Research Population:

Research Population
Adults

Citation:

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