<--- Back to Details
First PageDocument Content
Pediatrics / Mental retardation / Epidemiology / Newborn screening / Phenylketonuria / Galactosemia / Isovaleric acidemia / 2-Methylbutyryl-CoA dehydrogenase deficiency / 3-Methylcrotonyl-CoA carboxylase deficiency / Health / Medicine / Rare diseases
Date: 2014-09-09 13:55:11
Pediatrics
Mental retardation
Epidemiology
Newborn screening
Phenylketonuria
Galactosemia
Isovaleric acidemia
2-Methylbutyryl-CoA dehydrogenase deficiency
3-Methylcrotonyl-CoA carboxylase deficiency
Health
Medicine
Rare diseases

Annual Report2012_corrected.pub

Add to Reading List

Source URL: michigan.gov

Download Document from Source Website

File Size: 226,49 KB

Share Document on Facebook

Similar Documents

Pediatrics / Epidemiology / Newborn screening / Phenylketonuria / Association of Public Health Laboratories / Audiology / Screening / Medical genetics / Galactosemia / Medicine / Health / Medical specialties

NEWSLETTER SPRING-2015-Final.pub

DocID: 180UV - View Document

Newborn screening / Isovaleric acidemia / Methylmalonic acidemia / Acyl CoA dehydrogenase / Biotinidase deficiency / Galactosemia / Methylmalonic acid / Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency / Guthrie test / Health / Rare diseases / Medicine

Newborn Screening Year in Review 86,586 For Babies Born in 2013 Bloodspot Samples Received Initial

DocID: 14zTU - View Document

Rare diseases / Epidemiology / Newborn screening / Medical tests / Cystic fibrosis / Dried blood spot / Galactosemia / Phenylketonuria / Screening / Health / Medicine / Pediatrics

CDC’s Role in the Implementation of Newborn Screening Pilot Programs Activities of the Newborn Screening and Molecular Biology Branch Carla D. Cuthbert, Ph.D.

DocID: 12A2f - View Document

Newborn screening / Isovaleric acidemia / Galactosemia / Methylmalonic acidemia / Propionic acidemia / Malonyl-CoA decarboxylase deficiency / Inborn error of metabolism / Argininosuccinic aciduria / Organic acidemia / Health / Rare diseases / Medicine

TIMELINESS OF NEWBORN SCREENING – DACHDNC LABORATORY STANDARDS AND PROCEDURES SUBCOMMITTEE DRAFT FINDINGS AND PROPOSED RECOMMENDATIONS Kellie Kelm, PhD

DocID: 12v8A - View Document

Medical genetics / Newborn screening / Isovaleric acidemia / Propionic acidemia / Methylmalonic acidemia / Fatty-acid metabolism disorder / Very long-chain acyl-coenzyme A dehydrogenase deficiency / Galactosemia / Malonyl-CoA decarboxylase deficiency / Health / Rare diseases / Genetic genealogy

Timeliness of Newborn Screening – DACHDNC’s laboratory standards and procedures subcommittee draft findings

DocID: 12jOC - View Document