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Newborn Screening Programs and Projects
Division of Laboratory Sciences
Newborn Screening: Quality Assurance and Proficiency Testing for Newborn Screening
This CDC Program is a Voluntary, Non-regulatory Program to Help State Health Departments and their Laboratories Maintain and Enhance the Quality of Newborn Test Results
National Center on Birth Defects & Developmental Disabilities
Birth Defects: Newborn Screening and Related Conditions
Pediatric Genetics website, for Birth Defects at CDC, listing a number of activities and publications.
Early Hearing Detection and Intervention and Integration: Research Projects
Single Gene Disorders and Disability (SGDD): Newborn Screening Projects
Duchenne/Becker Muscular Dystrophy (DBMD) Screening and Diagnosis
Working with several partners to gather information on ways to improve screening and diagnosis for DBMD
Development of a newborn screening test for fragile X syndrome (FXS)
Developing an inexpensive and reliable screening test for FXS and testing de-identified blood spots from newborns to determine prevalence
Newborn Screening Publications
From Public Health Emergency to Public Health Service: The Implications of Evolving Criteria for Newborn Screening Panels
(2006)
Newborn Screening for Cystic Fibrosis
(2004)
MMWR, Evaluation of Benefits and Risks and Recommendations for State Newborn Screening Programs
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Page last updated: December 11, 2007
Content Source: National Office of Public Health Genomics
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National Office of Public Health Genomics, Centers for Disease Control and Prevention