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Propionic acidemia Propionyl-CoA carboxylase Genetic testing Prenatal diagnosis Health Medicine Rare diseases | J Med Genet 1999;36:412–[removed]Short reportsAdd to Reading ListSource URL: jmg.bmj.comDownload Document from Source WebsiteFile Size: 184,90 KBShare Document on Facebook |
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 |