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References American Board of Medical Geneticists. 2008a. Training options. training_options.shtml (accessed January 28, 2009). ———. 2008b. Specialties of genetics. (accessed January 28, 2009). ———. 2008c. Numbers of certified specialists in genetics—by specialty. http://www.abmg. org/pages/resources_byspecialty.htm (accessed January 29, 2009). Burke, W. 2008. Vision of the future. Presentation at Institute of Medicine workshop on in- novations in service delivery in the age of genomics. July 28. Washington, DC. Cabe, J., and S. Springer. 2008. National call to action on cancer prevention and survivorship. Tucson, AZ: Excel Print Communications. CDC (Centers for Disease Control and Prevention). 2000. National health information sur- vey cancer module. NHIS/2000/qcancerx.pdf. Cooksey, J. A., G. Forte, P. A. Flanagan, J. Benkendorf, and M. G. Blitzer. 2006. The medical genetics workforce: An analysis of clinical geneticist subgroups. Genet Med 8(10):603-614. DesRoches, C. M., E. C. Campbell, S. R. Rao, K. Donelan, T. G. Ferris, A. Jha, R. Kaushal, D. Levy, S. Rosenbaum, A. Shields, and D. Blumenthal. 2008. Electronic health record adoption in the ambulatory setting: Findings from a national survey of physicians. N Engl J Med 359:50-60. Deyo, R. A. 2002. Cascade effects of medical technology. Annu Rev Public Health 23:23-44. Eisenberg, J. M. 1999. Ten lessons for evidence-based technology assessment. JAMA 282(19): 1865-1869. Fiscella, K., and H. J. Geiger. 2006. Health information technology and quality improvement for community health centers. Health Aff 25(2):405-412. Gennaccaro, M., S. E. Waisbren, and D. Marsden. 2005. The knowledge gap in expanded newborn screening: Survey results from paediatricians in Massachusetts. J Inherit Metab Dis 28(6):819-824. 

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 INNOVATIONS IN SERVICE DELIVERY IN THE AGE OF GENOMICS Giardiello, F. M. 1997. Genetic testing in hereditary colorectal cancer. JAMA 278(15): 1278-1281. Gowda, G. A., S. Zhang, H. Gu, V. Asiago, N. Shanaiah, and D. Raftery. 2008. Metabolomics- based methods for early disease diagnostics. Expert Rev Mol Diagn 8(5):617-633. IOM. 1994. Assessing genetic risks: Implications for health and social policy. Washington, DC: National Academy Press. ———. 2000. America’s health care safety net: Intact but endangered. Washington, DC: National Academy Press. ———. 2001. Crossing the quality chasm. Washington, DC: National Academy Press. ———. 2003a. Who will keep the public healthy?: Educating public health professionals for the 21st century. Washington, DC: The National Academies Press. ———. 2003b. Unequal treatment: Confronting racial and ethnic disparities in health care. Washington, DC: The National Academies Press. Jarvinen, H. J., M. Aarnio, H. Mustonen, K. Aktan-Collan, L. A. Aaltonen, P. Peltomaki, A. De La Chapelle, and J. P. Mecklin. 2000. Controlled 15-year trial on screening for colorectal cancer in families with hereditary nonpolyposis colorectal cancer. Gastroen- terology 118(5):829-834. Korf, B. 2008. Brainstorming on a service delivery model for the future. Presentation at Insti- tute of Medicine workshop on innovations in service delivery in the age of genomics. July 28. Washington, DC. Korf, B. R., G. Feldman, and G. L. Wiesner. 2005. Report of Banbury Summit Meeting on train- ing of physicians in medical genetics, October 20-22, 2004. Genet Med 7(6):433-438. Korf, B. R., D. Ledbetter, and M. F. Murray. 2008. Report of the Banbury Summit Meet- ing on the evolving role of the medical geneticist, February 12-14, 2006. Genet Med 10(7):502-507. Latterich, M., M. Abramovitz, and B. Leyland-Jones. 2008. Proteomics: New technologies and clinical applications. Eur J Cancer 44(18):2737-2741. Levy, D. E., J. E. Garber, and A. E. Shields. (Unpublished). Underprovision of guideline recom- mended advice on genetic assessment of breast and ovarian cancer among U.S. women. Lochner Doyle, D., and C. Watts (Principal Investigators). 2008. Genetic services policy project final report. Seattle: Washington State Department of Health and the University of Washington. March of Dimes. 2007. Nearly 90 percent of babies receive recommended newborn screening tests. (accessed January 28, 2009). McGlynn, E. A., S. M. Asch, J. Adams, J. Keesey, J. Hicks, A. DeCristofaro, and E. A. Kerr. 2003. The quality of health care delivered to adults in the United States. N Engl J Med 348:2635-2645. Menasha, J. D., C. Schechter, and J. Willner. 2000. Genetic testing: A physician’s perspective. Mt Sinai J Med 67(2):144-151. National Library of Medicine. 2009. Colorectal cancer. colorectalcancer.html (accessed January 30, 2009). Ota Wang, V. 2008. The strengths and challenges of the current system: Patient education and communication. Presentation at Institute of Medicine workshop on innovations in service delivery in the age of genomics. July 28. Washington, DC. Parrott, S., and M. DelVecchio. 2007. Professional status survey 2006. National Society of Genetic Counselors, Inc. (ac- cessed January 30, 2009). Phelan, R., P. Borry, and H. C. Howard. 2008. Letter to the editor. Pers Med 5(5):425-426. Rosenbaum, S., P. Shin, and J. Darnell. 2004. Economic stress and the safety net: A health center update. Washington, DC: The Henry J. Kaiser Family Foundation.

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