Subchapter IX. Genetic Diseases, Hemophilia Programs, and Sudden Infant Death Syndrome
Part A. Genetic Diseases
- 42 U.S.C. § 300b Repealed
- 42 U.S.C. § 300b-1 Research Project Grants and Contracts
- 42 U.S.C. § 300b-2 Voluntary Participation By Individuals
- 42 U.S.C. § 300b-3 Application; Special Consideration to Prior Sickle Cell Anemia Grant Recipients
- 42 U.S.C. § 300b-4 Public Health Service Facilities
- 42 U.S.C. § 300b-5 Repealed
- 42 U.S.C. § 300b-6 Applied Technology
- 42 U.S.C. § 300b-7 Tourette Syndrome
- 42 U.S.C. § 300b-8 Improved Newborn and Child Screening For Heritable Disorders
- 42 U.S.C. § 300b-9 Evaluating the Effectiveness of Newborn and Child Screening and Followup Programs
- 42 U.S.C. § 300b-10 Advisory Committee On Heritable Disorders In Newborns and Children
- 42 U.S.C. § 300b-11 Clearinghouse of Newborn Screening Information
- 42 U.S.C. § 300b-12 Laboratory Quality and Surveillance
- 42 U.S.C. § 300b-13 Interagency Coordinating Committee On Newborn and Child Screening
- 42 U.S.C. § 300b-14 National Contingency Plan For Newborn Screening
- 42 U.S.C. § 300b-15 Hunter Kelly Research Program
- 42 U.S.C. § 300b-16 Authorization of Appropriations For Newborn Screening Programs and Activities
- 42 U.S.C. § 300b-17 Report By Secretary
Part C. Hemophilia Programs