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Biotinidase
Results: 180

#	Item
151	Microsoft Word - Rhode Island Insert English FINAL.doc Add to Reading List Source URL: www.nergg.org Language: English - Date: 2007-10-17 09:01:25 Medical genetics Newborn screening Isovaleric acidemia Propionic acidemia 3-Methylcrotonyl-CoA carboxylase deficiency Methylmalonic acidemia Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Biotinidase deficiency Very long-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Genetic genealogy
152	Center for Congenital & Inherited Disorders Why does IDPH store residual newborn screening specimens What is newborn blood spot screening? Add to Reading List Source URL: www.idph.state.ia.us Language: English - Date: 2010-07-29 16:02:49 Rare diseases Epidemiology Newborn screening Phenylketonuria Medical genetics Biotinidase deficiency Cystic fibrosis Sickle-cell disease Biotin Health Medicine Pediatrics
153	Microsoft Word - biotinidase Add to Reading List Source URL: www.idph.state.ia.us Language: English - Date: 2007-06-25 16:35:52 Genetic genealogy Multiple carboxylase deficiency Biotinidase Biotin Rare diseases Newborn screening Biotin deficiency Holocarboxylase synthetase deficiency Health Genetics Biotinidase deficiency
154	PARENT’S GUIDE TO YOUR BABY’S NEWBORN SCREENING Add to Reading List Source URL: dhhs.ne.gov Language: English - Date: 2014-03-25 08:53:10 Newborn screening Phenylketonuria Screening Biotinidase deficiency March of Dimes Galactosemia Glutaric aciduria type 1 Genetic testing Cystic fibrosis Health Medicine Rare diseases
155	Heel Stick News January 2005 Add to Reading List Source URL: www.idph.state.ia.us Language: English - Date: 2007-06-25 16:37:18 Genetic genealogy Pediatrics Newborn screening Guthrie test Phenylketonuria Neonatal heel prick Biotinidase deficiency Fatty-acid metabolism disorder Medium-chain acyl-coenzyme A dehydrogenase deficiency Health Medicine Rare diseases
156	July 2003 Heel Stick Newsletter Add to Reading List Source URL: www.idph.state.ia.us Language: English - Date: 2007-06-25 16:37:19 Mental retardation Epidemiology Newborn screening Medical genetics Biotinidase deficiency Phenylketonuria Galactosemia Neonatal heel prick Congenital hypothyroidism Medicine Health Pediatrics
157	IDPH logo final panton 294 Add to Reading List Source URL: www.idph.state.ia.us Language: English - Date: 2010-02-10 11:12:42 Rare diseases Epidemiology Newborn screening Phenylketonuria Medical genetics Biotinidase deficiency Cystic fibrosis Sickle-cell disease Biotin Health Medicine Pediatrics
158	Iowa Newborn Screening Program Report for Calendar Year 2011 Short Term and Long Term Follow Up Report The following report describes the purpose, processes and activities of the short term and long term follow up progr Add to Reading List Source URL: www.idph.state.ia.us Language: English - Date: 2013-09-04 08:31:29 Rare diseases Pediatrics Inborn errors of carbohydrate metabolism Epidemiology Newborn screening Mental retardation Galactosemia Biotinidase deficiency Fatty-acid metabolism disorder Health Medicine Genetic genealogy
159	Hygienic Laboratory The University of Iowa For Questions About Resubmission and Result Interpretation Contact Medical Consultants LABORATORY HOSPITAL Add to Reading List Source URL: www.idph.state.ia.us Language: English - Date: 2007-06-25 16:38:00 Rare diseases Newborn screening Fatty-acid metabolism disorder Biotinidase deficiency Propionic acidemia 3-Methylcrotonyl-CoA carboxylase deficiency Carnitine palmitoyltransferase I 2-Methylbutyryl-CoA dehydrogenase deficiency Isovaleric acidemia Health Genetic genealogy Medical genetics
160	Cloud Mask (35_L2) (Updated[removed]Steven Ackerman, Rick Frey Add to Reading List Source URL: modis-atmos.gsfc.nasa.gov Language: English - Date: 2011-04-28 08:00:36 Moderate-Resolution Imaging Spectroradiometer EVI Cloud Biotinidase Planetary science Spaceflight Normalized Difference Vegetation Index Remote sensing Earth