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). Pediatrics May;148(5):577-584.
- 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.