Author:
Leppert Kristen,Bisordi Katharine,Nieto Jessica,Maloney Kristin,Guan Yue,Dixon Shannan,Egense Alena
Reference14 articles.
1. Andrews, L. B., Fullarton, J. E., Holtzman, N. A., & Motulsky G for the Institute of Medicine, Committee on Assessing Genetic Risks. (1994). Assessing genetic risk: implications for health and social policy. Washington, DC: National Academy Press.
2. Baby’s First Test (2015). Retrieved from
http://www.babysfirsttest.org
.
3. Farrell, M. H., & Christopher, S. A. (2013). Frequency of high-quality communication behaviors used by primary care providers of heterozygous infants after newborn screening. Patient Education and Counseling, 90(2), 226–232.
4. Farrell, M., Certain, L., & Farrell, P. (2001). Genetic counseling and risk communication services of newborn screening programs. Archives of Pediatrics & Adolescent Medicine, 155(2), 120–126.
5. Hayeems, R. Z., Bytautas, J. P., & Miller, F. A. (2008). A systematic review of the effects of disclosing carrier results generated through newborn screening. Journal of Genetic Counseling, 17(6), 538–549 12p.
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