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2020 US Code
Title 42 - The Public Health and Welfare
Chapter 6A - Public Health Service
Subchapter IX - Genetic Diseases, Hemophilia Programs, and Sudden Infant Death Syndrome
Part A - Genetic Diseases
United States Code, 2018 Edition, Supplement 2, Title 42 - THE PUBLIC HEALTH AND WELFARE |
Bills and Statutes |
United States Code |
Y 1.2/5: |
Title 42 - THE PUBLIC HEALTH AND WELFARE CHAPTER 6A - PUBLIC HEALTH SERVICE SUBCHAPTER IX - GENETIC DISEASES, HEMOPHILIA PROGRAMS, AND SUDDEN INFANT DEATH SYNDROME Part A - Genetic Diseases |
sections 300b to 300b-17 |
2020 |
January 13, 2021 |
No |
standard |
86 Stat. 652 90 Stat. 407 |
Public Law 92-414, Public Law 94-278 |
- Sec. 300b - Repealed. Pub. L. 97-35, title XXI, ยง2193(b)(1), Aug. 13, 1981, 95 Stat. 827
- Sec. 300b-1 - Research project grants and contracts
- Sec. 300b-2 - Voluntary participation by individuals
- Sec. 300b-3 - Application; special consideration to prior sickle cell anemia grant recipients
- Sec. 300b-4 - Public Health Service facilities
- Sec. 300b-5 - Sickle cell disease and other heritable blood disorders research, surveillance, prevention, and treatment
- Sec. 300b-6 - Applied technology
- Sec. 300b-7 - Tourette Syndrome
- Sec. 300b-8 - Improved newborn and child screening for heritable disorders
- Sec. 300b-9 - Evaluating the effectiveness of newborn and child screening and followup programs
- Sec. 300b-10 - Advisory Committee on Heritable Disorders in Newborns and Children
- Sec. 300b-11 - Clearinghouse of newborn screening information
- Sec. 300b-12 - Laboratory quality and surveillance
- Sec. 300b-13 - Interagency Coordinating Committee on Newborn and Child Screening
- Sec. 300b-14 - National contingency plan for newborn screening
- Sec. 300b-15 - Hunter Kelly Research Program
- Sec. 300b-16 - Authorization of appropriations for newborn screening programs and activities
- Sec. 300b-17 - Report by Secretary
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