Assessing the Informational Needs of Adolescents with a Genetic Condition: What Do They Want to Know?

Author:

Szybowska Marta,Hewson Stacy,Antle Beverley J.,Babul-Hirji Riyana

Publisher

Wiley

Subject

Genetics(clinical)

Reference24 articles.

1. Ackard, D. M., & Neumark-Sztainer, D. (2001). Health care information sources for adolescents: Age and gender differences on use, concerns, and needs. J. Adolesc. Health, 29, 170–176.

2. American Academy of Pediatrics, American Academy of Family Physicians, & American College of Physicians-American Society of Internal Medicine. (2002). A consensus statement on health care transitions for young adults with special health care needs. Pediatrics, 110(6), 1304–1306.

3. Antle, B. J., Anderson, D., Phillips, H., & Feigenbaum, A. (2001). More on my own: A transition education and planning project–Final report to the Garrod Association. Toronto: The Hospital for Sick Children.

4. Beresford, B. A., & Sloper, P. (2003). Chronically Ill adolescents’ experiences of communicating with doctors: A qualitative study. J. Adolesc. Health, 33, 172–179.

5. Biesecker, B. B., & Peters, K. F. (2001). Process studies in genetic counseling: peering into the black box. Am. J. Med. Genet, 106(3), 191–198.

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