Be Ready to Talk With Parents About Direct-to-Consumer Genetic Testing
Author:
Affiliation:
1. Center for Biomedical Ethics and Society, Department of Pediatrics, Vanderbilt University Medical Center, Nashville, Tennessee
Publisher
American Medical Association (AMA)
Subject
Pediatrics, Perinatology and Child Health
Link
https://jamanetwork.com/journals/jamapediatrics/articlepdf/2757557/jamapediatrics_clayton_2019_vp_190033.pdf
Reference7 articles.
1. The impact of communicating genetic risks of disease on risk-reducing health behaviour: systematic review with meta-analysis.;Hollands;BMJ,2016
2. False-positive results released by direct-to-consumer genetic tests highlight the importance of clinical confirmation testing for appropriate patient care.;Tandy-Connor;Genet Med,2018
3. Behavioural changes, sharing behaviour and psychological responses after receiving direct-to-consumer genetic test results: a systematic review and meta-analysis.;Stewart;J Community Genet,2018
4. Consumer perceptions of interactions with primary care providers after direct-to-consumer personal genomic testing.;van der Wouden;Ann Intern Med,2016
5. Direct-to-consumer genetic testing: user motivations, decision making, and perceived utility of results.;Roberts;Public Health Genomics,2017
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