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3135.0: Monday, November 8, 2004: 10:30 AM-12:00 PM | |||
Oral | |||
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This session will provide an understanding of the public health implications of genetics from state activities in newborn screening, genetics services and policy development to national initiatives with education and an exploration of complex health insurance implications of the human genome project. | |||
Learning Objectives: At the end of the session participants will have: a. An understanding of the public health implications of genetics b. An understanding of the policy and programmatic components of state activities in newborn screening. c. An understanding of the roles of key stakeholders in genetic testing, service and policy development d. A recognition of common disorders and there genetic components e. A recognition of key issues related to the practices and policies of health maintenance organizations related to services for individuals with disabilities | |||
Penny Kyler | |||
Penny Kyler, MA, OTR | |||
Introductory Remarks | |||
Expanded newborn screening: The Mississippi experience Daniel Bender, MHS, Jerry McClure, BS, Marianne E Zotti, DrPH, RN, Tom Carey, MD | |||
Genetics Plan for Connecticut: Process and Development Carol L. Stone, PhD, Beverly Burke, MSW, Meg Hooper, MPA | |||
Website expansion for the Tennessee genetics and newborn screening program David Hollar, PhD, Teresa Blake, MS, Beth Wilson, MS, MPH, Carmen Lozzio, MD | |||
Human Genome Project and health insurance: Implications for families Virginia L. Miller, DrPH, Angela Martin, MSW, David R. Moss, JD | |||
Prenatal genetic screening with an interactive computer program Jennifer M. Griffith, DrPH, MPH, James R. Sorenson, PhD, Tracey Grant, MS, J. Michael Bowling, PhD | |||
See individual abstracts for presenting author's disclosure statement and author's information. | |||
Organized by: | Maternal and Child Health | ||
CE Credits: | CME, Health Education (CHES), Nursing |