2011 Newborn Screening data as of August 2012.xlsx

First Page		Document Content
Date: 2012-09-04 18:41:39 Medical genetics Newborn screening Propionic acidemia Methylmalonic acidemia Isovaleric acidemia Glutaric aciduria type 1 Medium-chain acyl-coenzyme A dehydrogenase deficiency Biotinidase deficiency Maple syrup urine disease Health Rare diseases Genetic genealogy		2011 Newborn Screening data as of August 2012.xlsx Add to Reading List Source URL: azdhs.gov Download Document from Source Website File Size: 62,08 KB Share Document on Facebook

	Newborn Screening Year in Review 86,586 For Babies Born in 2013 Bloodspot Samples Received Initial DocID: 14zTU - View Document
	Newborn Screening Year in Review 86,586 For Babies Born in 2013 Bloodspot Samples Received Initial DocID: 11G3r - View Document
	Chart of Metabolic Disorders Screened Table of Disorders Screened by Program Condition Incidence DocID: Z5KR - View Document
	American College of Medical Genetics ACT SHEET Newborn Screening ACT Sheet DocID: Ri0X - View Document
	CYTOGENETIC STUDIES ROUTINE AND HIGH RESOLUTION BLOOD Collect 4-6 mls of peripheral blood in a green top sodium heparin tube. Please do not used lithium heparin or ammonium heparin as these can be toxic to the cells. Tra DocID: O1GM - View Document