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Resources: Newborn Screening
American College of Medical Genetics
Case Management for Children & Pregnant Women
Children With Special Health Care Needs (CSHCN) Services Program Gurian, E.A., Kinnamon, D.D., Henry, J.J. & Waisbren, S.E. (2006). Expanded newborn screening for biochemical disorders: the effect of a false-positive result.
Pediatrics 117(6), 1915-21.
March of Dimes Quick Reference and Fact Sheets Marsden, D., Larson, C. & Levy, H.L. Newborn screening for metabolic disorders. (2006).
May;148(5):577-584. Pediatrics Raghuveer, T.S., Garg, U. & Graf, W.D. (2006). Inborn errors of metabolism in infancy and early childhood: an update
. American Family Physician Jun 1;73(11):1981-90.
National Newborn Screening & Genetics Resource Center
Newborn Screening Case Management Program Tarini, B.A., Christakis, D.A. & Welch H.G. (2006). State newborn screening in the tandem mass spectrometry era: more tests, more false-positive results.
Pediatrics 118(2), 448-56.
Texas Department of State Health Services, map of regional offices Zytkovicz, T.H., Fitzgerald, E.F., Marsden, D., Larson, C.A., Shih, V.E., Johnson, D.M., ... Grady G.F. (2001). Tandem mass spectrometric analysis for amino, organic, and fatty acid disorders in newborn dried blood spots: a two-year summary from the New England newborn screening program.
Clinical Chemistry 47, 1945-55.
Nationally recognized by ASTHO for creative approaches to public health needs by state health programs and initiatives.