[Simultaneous thin-layer chromatography of blood and urine samples for the diagnosis of hereditary amino acid metabolism disorders]

MeSH terms

• Amino Acid Metabolism, Inborn Errors / diagnosis*
• Amino Acid Metabolism, Inborn Errors / genetics
• Amino Acid Metabolism, Inborn Errors / metabolism
• Chromatography, Thin Layer
• Consanguinity
• Galactosemias / diagnosis
• Homocystinuria / diagnosis
• Humans
• Maple Syrup Urine Disease / diagnosis
• Mucopolysaccharidoses / diagnosis
• Phenylketonurias / diagnosis