The Changing Age of Individuals Seeking Presymptomatic Genetic Testing for Huntington Disease
Author:
Funder
National Center for Advancing Translational Sciences
Publisher
Wiley
Subject
Genetics(clinical)
Link
http://link.springer.com/article/10.1007/s10897-018-0233-9/fulltext.html
Reference15 articles.
1. Aro, A., Hakonen, A., & Hietala, M. (1997). Acceptance of genetic testing in a general population: age, education and gender differences. Patient Education and Counseling, 32, 41–49.
2. Dufrasne, S., Roy, M., Galvez, M., & Rosenblatt, D. (2011). Experience over fifteen years with a protocol for predictive testing for Huntington disease. Molecular Genetics and Metabolism, 102, 494–504.
3. Duncan, R., Gillam, L., Savulescu, J., Williamson, R., Rogers, J., & Delatycki, M. (2007). “Holding your breath”: interviews with young people who have undergone predictive genetic testing for Huntington disease. American Journal of Medical Genetics, 143A, 1984–1989.
4. Fischer, E., & Hayden, M. (2014). Multisource ascertainment of Huntington disease in Canada: prevalence and population at risk. Movement Disorders, 29, 105–114.
5. Koutsis, G., Karadima, G., Kladi, A., & Panas, M. (2014). Late-onset Huntington’s disease: diagnostic and prognostic considerations. Parkinsonism & Related Disorders, 20, 726–730.
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