![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 / Phenylketonuria / Galactosemia / Neonatal jaundice / Galactose-1-phosphate uridylyltransferase deficiency / Screening / Congenital adrenal hyperplasia due to 21-hydroxylase deficiency / Neonatology / Cystic fibrosis / Medicine / Health / Pediatrics](/pdf-icon.png) Date: 2012-07-24 10:19:31Newborn 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. _VaAdd to Reading ListSource URL: genes-r-us.uthscsa.eduDownload Document from Source Website File Size: 276,00 KBShare Document on Facebook
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