Volume：
30
Issue：
1
Page：
65-75
Publication year：
Jul. 31, 2019
JST Material Number：
L4006A
ISSN：
1343-0203
Document type：
Article
Country of issue：
Japan (JPN)
Language：
JAPANESE (JA)
Reference (35)：
Bonnie, L. H., 2003, Talking to Kids about Huntington’s Disease: A Book for People Who Knew Children with HD in Their Family.
Daly, M. B., Montgomery, S., Bingler, R., and Ruth, K., 2016, “Communicating Genetic Test Results within the Family: Is It Lost in Translation? A Survey of Relatives in the Randomized Six-step Study,” Familial Cancer, 15(4): 697-706.
Dure, L. S., Quaid, K., and Beasley, T. M., 2008, “A Pilot Assessment of Parental Practices and Attitudes Regarding Risk Disclosure and Clinical Research Involving Children in Huntington Disease Families,” Genetics in Medicine, 10(11): 811-819.
Forrest, K., Simpson, S. A., Wilson, B. J., Van Teijlingen, E. R., McKee, L., Haites, N., and Matthews, E., 2003, “To Tell or Not to Tell: Barriers and Facilitators in Family Communication about Genetic Risk,” Clinical Genetics, 64(4): 317-326.
Forrest Keenan, K., Simpson, S. A., Wilson, B. J., Van Teijlingen, E. R., McKee, L., Haites, N., and Matthews, E., 2005, “It’s Their Blood Not Mine: Who’s Responsible for (Not) Telling Relatives about Genetic Risk?” Health Risk & Society, 7(3): 209-226.
