Disorders and Reference Ranges

First Page		Document Content
Date: 2014-12-15 13:01:02 Medical genetics Newborn screening Isovaleric acidemia Methylmalonic acidemia Propionic acidemia Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Fatty-acid metabolism disorder Acyl CoA dehydrogenase Very long-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Genetic genealogy		Disorders and Reference Ranges Add to Reading List Source URL: www.azdhs.gov Download Document from Source Website File Size: 103,94 KB Share Document on Facebook

	TIMELINESS OF NEWBORN SCREENING – DACHDNC LABORATORY STANDARDS AND PROCEDURES SUBCOMMITTEE DRAFT FINDINGS AND PROPOSED RECOMMENDATIONS Kellie Kelm, PhD DocID: 12v8A - View Document
	Timeliness of Newborn Screening – DACHDNC’s laboratory standards and procedures subcommittee draft findings DocID: 12jOC - View Document
	J Med Genet 1999;36:412–[removed]Short reports DocID: 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