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United States Code (Last Updated: May 24, 2014) |
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Title 42. THE PUBLIC HEALTH AND WELFARE |
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Chapter 6A. PUBLIC HEALTH SERVICE |
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SubChapter IX. GENETIC DISEASES, HEMOPHILIA PROGRAMS, AND SUDDEN INFANT DEATH SYNDROME |
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Part A. Genetic Diseases |
§ 300b. Repealed. Pub. L. 97–35, title XXI, § 2193(b)(1), |
§ 300b–1. Research project grants and contracts |
§ 300b–2. Voluntary participation by individuals |
§ 300b–3. Application; special consideration to prior sickle cell anemia grant recipients |
§ 300b–4. Public Health Service facilities |
§ 300b–5. Repealed. Pub. L. 97–35, title XXI, § 2193(b)(4), |
§ 300b–6. Applied technology |
§ 300b–7. Tourette Syndrome |
§ 300b–8. Improved newborn and child screening for heritable disorders |
§ 300b–9. Evaluating the effectiveness of newborn and child screening programs |
§ 300b–10. Advisory Committee on Heritable Disorders in Newborns and Children |
§ 300b–11. Clearinghouse of newborn screening information |
§ 300b–12. Laboratory quality |
§ 300b–13. Interagency Coordinating Committee on Newborn and Child Screening |
§ 300b–14. National contingency plan for newborn screening |
§ 300b–15. Hunter Kelly Research Program |
Amendments
1976—Pub. L. 94–278, title IV, § 403(a),