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Newborn screening / Phenylketonuria / Galactosemia / Neonatal jaundice / Galactose-1-phosphate uridylyltransferase deficiency / Screening / Congenital adrenal hyperplasia due to 21-hydroxylase deficiency / Neonatology / Cystic fibrosis / Medicine / Health / Pediatrics
Date: 2012-07-24 10:19:31
Newborn screening
Phenylketonuria
Galactosemia
Neonatal jaundice
Galactose-1-phosphate uridylyltransferase deficiency
Screening
Congenital adrenal hyperplasia due to 21-hydroxylase deficiency
Neonatology
Cystic fibrosis
Medicine
Health
Pediatrics

Newborn Screening Articles Spring[removed]_Clin_Chim_Acta._ 2012 Jul 11;[removed]):[removed]Epub 2012 Mar 23. Amino acid disorders detected by quantitative amino acid HPLC analysis in Thailand: An eight-year experience. _Va

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