Medicine & Life Sciences
Neonatal Screening
Phenylketonurias
Advisory Committees
Newborn Infant
Child
Glycogen Storage Disease Type I
Spinal Muscular Atrophy
Medical Genetics
Fibroblasts
Prenatal Diagnosis
Inborn Genetic Diseases
Menkes Kinky Hair Syndrome
Mucopolysaccharidoses
Uric Acid
Glycogen Storage Disease
Glycogen Storage Disease Type IV
Maternal Phenylketonuria
Duchenne Muscular Dystrophy
Congresses
Phenylalanine
Metachromatic Leukodystrophy
Liver
Glycogen Storage Disease Type II
Amniotic Fluid
1,4-alpha-Glucan Branching Enzyme
Copper
Glucose-6-Phosphatase
Sabinas brittle hair syndrome
Mucopolysaccharidosis I
Gout
Skin
Health Services
Therapeutics
Hepatorenal form of glycogen storage disease
Inborn Errors Metabolism
Hair
Amino Acids
Mucopolysaccharidosis IV
Histidinemia
Mannosidase Deficiency Diseases
Pili Torti
1,4-glucan
Trace Elements
Transferases
United States Dept. of Health and Human Services
Enzymes
Neurotransmitter Agents
Maternal Health
Chemical Compounds
trimethylchlorosilane
hexamethylsilazane
Human Milk
Phenylacetates
Phenylalanine
phenylacetylglutamine
Glucose-6-Phosphatase
Inorganic Pyrophosphatase
Metabolism
Arylsulfatases
Glycogen
Carbamyl Phosphate
Cerebroside-Sulfatase
Fibroblasts
Hydroxylamine
Hydrolysis
Metabolites
Copper
diphosphoric acid
X-Ray Emission Spectrometry
pyridine
Gas chromatography
Trace Elements
