Newborn - PDFSEARCH.IO - Document Search Engine

Newborn
Results: 3932

#	Item
991	July[removed]KY Division of Laboratory Services Reference List of Tests ACYLCARNITINES DLS Department: Add to Reading List Source URL: chfs.ky.gov Language: English - Date: 2014-12-08 17:56:37 Rare diseases Hoffmann-La Roche Molecular biology Polymerase chain reaction Type Methylmalonic acidemia Newborn screening Microbiological culture Biology Health Science
992	pl More than 95 percent of newborns who are born deaf have parents with normal hearing. Hearing loss is invisible; it cannot be seen by examining your newborn’s ears. Add to Reading List Source URL: www.audiology.org Language: English - Date: 2014-08-18 15:08:51 Hearing Audiology Auditory system Hearing impairment Infant Hearing test Congenital hearing loss Marion Downs Medicine Health Otology
993	Microsoft Word - SCAD.doc Add to Reading List Source URL: health.mo.gov Language: English - Date: 2007-09-14 09:00:00 Fatty-acid metabolism disorder Newborn screening Fatty acid metabolism Short-chain acyl-coenzyme A dehydrogenase deficiency Medium-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Medicine
994	Phenylketonuria (PKU) What is Phenylketonuria? Phenylketonuria (also known as PKU) is an inherited condition that affects the way a person’s body uses protein. A person with PKU cannot use a component of protein called Add to Reading List Source URL: health.state.tn.us Language: English - Date: 2007-05-01 15:48:27 Mental retardation Phenylketonuria PKU Phenylalanine Dominance Hyperphenylalanemia Medical genetics Newborn screening Tetrahydrobiopterin deficiency Medicine Health Biology
995	Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD) Add to Reading List Source URL: health.mo.gov Language: English - Date: 2009-02-03 16:51:42 Genetic genealogy Glutaric acidemia type 2 Fatty-acid metabolism disorder Glutaric aciduria type 1 Newborn screening Fatty acid metabolism Propionic acidemia Very long-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Medicine
996	1 STATE OF TENNESSEE NEWBORN SCREENING PROGRAM Add to Reading List Source URL: health.state.tn.us Language: English - Date: 2011-09-09 15:00:52 Hematopathology Hemoglobins Sickle-cell disease Thalassemia Sickle cell trait Hematologic disease Acute chest syndrome Hemoglobin Hemolysis Medicine Health Hematology
997	Cystic Fibrosis Mutation Detection Quarterly Report PROFICIENCY TESTING August 2014 Add to Reading List Source URL: www.cdc.gov Language: English - Date: 2014-09-16 09:39:27 Molecular biology Pediatrics Rare diseases Biotechnology Cystic fibrosis Newborn screening High Resolution Melt Allele-specific oligonucleotide Hologic Biology Health Genetics
998	Isovaleric Acidemia (IVA) An organic acid disorder What is it? Isovaleric Acidemia (also known as IVA) is an inherited organic acid disorder. People with organic acid disorders, like IVA, cannot properly break down certa Add to Reading List Source URL: health.mo.gov Language: English - Date: 2007-09-13 16:17:12 Medical genetics Isovaleric acidemia Newborn screening Organic acidemia Propionic acidemia Methylmalonic acidemia Health Rare diseases Genetic genealogy
999	Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD) Add to Reading List Source URL: health.mo.gov Language: English - Date: 2009-02-03 16:51:01 Medical genetics Methylmalonic acidemia Propionic acidemia Organic acidemia Newborn screening Methylmalonic acid Malonyl-CoA decarboxylase deficiency Vitamin B12 Isovaleric acidemia Health Rare diseases Genetic genealogy
1000	Request for Applications RFA #A-293 Genetics Services FUNDING AGENCY: North Carolina Department of Health and Human Services, Add to Reading List Source URL: www.ncdhhs.gov Language: English Medical specialties Genetic counseling Newborn screening Medicaid Health insurance Health care provider Program for Jewish Genetic Health Public health genomics Medicine Health Medical genetics

UPDATE