Author:
Xhelili Ciaccio Marisola,Dumaine Drew
Publisher
Springer International Publishing
Reference24 articles.
1. Brandt, Jason, Kimberly A. Quaid, Susan E. Folstein, Paul Garber, Nancy E. Maestri, Margaret H. Abbott, Phillip R. Slavney, Mary L. Franz, Laura Kasch, and Haig H. Kazazian. 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.
2. Divion, Victoria, Mitch DeKoven, John H. Warner, Joseph Giuliano, Karen E. Anderson, Douglas Langbehn, and Won Chan Lee. 2013. The direct medical costs of Huntington’s disease by stage. A retrospective commercial and Medicaid claims data analysis. Journal of Medical Economics 16 (8): 1043–1050.
3. Etchegary, Holly. 2011. Healthcare experiences of families affected by Huntington disease: Need for improved care. Chronic Illness 7: 225–238.
4. Hawkins, Alice K., and Michael R. Hayden. 2011. A grand challenge: Providing benefits of clinical genetics to those in need. Genetics in Medicine 13: 197–200.
5. Huntington’s disease society of America. 2016. Genetic testing protocol for Huntington’s disease. http://hdsa.org/wp-content/uploads/2015/02/HDSA-Gen-Testing-Protocol-for-HD.pdf. Accessed 21 Dec 2018.