Subpart A - GENETIC CONDITIONS AND NEWBORNS
- Section 40:1081.1 - Programs for combating phenylketonuria, congenital hypothyroidism, galactosemia, sickle cell diseases, biotinidase deficiency, and other genetic conditions
- Section 40:1081.2 - Tests
- Section 40:1081.3 - Cooperation with the Louisiana Department of Health
- Section 40:1081.4 - Cooperation of physicians and hospitals
- Section 40:1081.5 - Redesignated
- Section 40:1081.6 - Redesignated
- Section 40:1081.7 - Redesignated
- Section 40:1081.8 - Redesignated
- Section 40:1081.9 - Hemophilia; state treatment program; advisory committee
- Section 40:1081.10 - Privacy of genetic information
- Section 40:1081.11 - Krabbe disease; public information
- Section 40:1081.12 - Medicaid coverage; genetic testing of critically ill infants