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![]() Date: 2012-04-12 12:46:55Medical genetics Newborn screening Methylmalonic acidemia Isovaleric acidemia Propionic acidemia Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Methylmalonic acid Maple syrup urine disease Acyl CoA dehydrogenase Health Rare diseases Genetic genealogy | Add to Reading List |
![]() | TIMELINESS OF NEWBORN SCREENING – DACHDNC LABORATORY STANDARDS AND PROCEDURES SUBCOMMITTEE DRAFT FINDINGS AND PROPOSED RECOMMENDATIONS Kellie Kelm, PhDDocID: 12v8A - View Document |
![]() | Timeliness of Newborn Screening – DACHDNC’s laboratory standards and procedures subcommittee draft findingsDocID: 12jOC - View Document |
![]() | J Med Genet 1999;36:412–[removed]Short reportsDocID: NHX0 - View Document |
![]() | 2013 General Session - Introduced Version - HB0145 - Insurance-coverage of phenylketonuria.DocID: NC55 - View Document |
![]() | 2013 General Session - Engrossed Version - HB0145 - Insurance-coverage of inherited enzymatic disorders.DocID: NxPs - View Document |