Repealed by SL 1978, ch 253 , § 2

SDCL § 34-24-12 — under CHILD HEALTH.

SDCL § 34-24-12

34-24-13 34-24-13 to 34-24-15. Repealed by SL 2013, ch 154 , §§ 43 to 45. 34-24-16 Educational program on metabolic diseases. 34-24-17 Screening of newborn infants for metabolic, inherited, and genetic disorders. 34-24-18 Phenylketonuria, hypothyroidism, and galactosemia testing in newborn. 34-24-19 Phenylketonuria, hypothyroidism, or galactosemia tests when facilities not available. 34-24-20 Phenylketonuria, hypothyroidism and galactosemia tests provided by department for newborn not tested. 34-24-21 Procedures prescribed after positive phenylketonuria, hypothyroidism, or galactosemia tests. 34-24-22 Testing for other metabolic, inherited, or genetic disorders. 34-24-23 Results of tests for metabolic, inherited, or genetic disorders reported to department. 34-24-24 Information to be provided to parents or guardians. 34-24-25 Rules and regulations. 34-24-26