Perspectives on Genetic Testing and Return of Results from the First Cohort of Presymptomatically Tested Individuals At Risk of Huntington Disease
Author:
Funder
National Human Genome Research Institute
Publisher
Wiley
Subject
Genetics (clinical)
Link
http://link.springer.com/article/10.1007/s10897-018-0274-0/fulltext.html
Reference27 articles.
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2. ACMG Board of Directors. (2016). Direct-to-consumer genetic testing: a revised position statement of the American College of Medical Genetics and Genomics. Genetics in Medicine, 18(2), 207–208. https://doi.org/10.1038/gim.2015.190 .
3. Baig, S. S., Strong, M., Rosser, E., Taverner, N. V., Glew, R., Miedzybrodzka, Z., Clarke, A., et al. (2016). Twenty-two years of predictive testing for Huntington's disease: the experience of the UK Huntington’s Prediction Consortium. European Journal of Human Genetics, 24(10), 1396–1402. https://doi.org/10.1038/ejhg.2016.36 .
4. Brandt, J., Quaid, K. A., Folstein, S. E., Garber, P., Maestri, N. E., Abbott, M. H. et al., (1989). Presymptomatic diagnosis of delayed-onset disease with linked DNA markers. The experience in Huntington’s disease. Journal of the American Medical Association, 261(21), 3108–3114.
5. Codori, A. M., & Brandt, J. (1994). Psychological costs and benefits of predictive testing for Huntington’s disease. American Journal of Medical Genetics, 54(3), 174–184.
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