Chapter 4 : Newborn Screening Almost every child born in the United States undergoes state-mandated newborn screening. For each state, a small blood sample (“heel stick”) is collected from each newborn within 48 hou

First Page		Document Content
Date: 2013-10-04 10:41:36 Genetic genealogy Pediatrics Newborn screening Methylmalonic acidemia Neonatal heel prick Galactosemia Biotinidase deficiency 2-Methylbutyryl-CoA dehydrogenase deficiency Hyperammonemia Health Medicine Rare diseases		Chapter 4 : Newborn Screening Almost every child born in the United States undergoes state-mandated newborn screening. For each state, a small blood sample (“heel stick”) is collected from each newborn within 48 hou Add to Reading List Source URL: www.geneticalliance.org Download Document from Source Website File Size: 113,62 KB Share Document on Facebook

	IMD Program List of Disorders, Covered Drugs, Supplements and Specialty Foods DocID: 1qvPf - View Document
	physician fact sheet Medium-Chain Acyl-Coenzyme A Dehydrogenase Deficiency (MCAD) Dr Janice Fletcher, MD, FRACP, BSc, Clinical Geneticist (HGSA), FRCPA DocID: W6MK - View Document
	HK J Paediatr (new series) 2004;9:[removed]A Baby with Nonketotic Hyperglycinaemia HNT HUI, YC HO, HB CHAN, SCF TAM, NLS TANG, PLS IP DocID: VyHh - View Document
	UCDC Newsletter_4.22.13_Final.pub DocID: HWNL - View Document
	Ottobre[removed]Elenchi dei prodotti medicinali per le malattie rare in Europa* DocID: HEZu - View Document