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Newborn screening / Screening / Cystic fibrosis / Genetic testing / Congenital hypothyroidism / Phenylketonuria / Neonatology / Prenatal diagnosis / Group B streptococcal infection / Medicine / Health / Pediatrics
Date: 2012-07-24 10:18:35
Newborn screening
Screening
Cystic fibrosis
Genetic testing
Congenital hypothyroidism
Phenylketonuria
Neonatology
Prenatal diagnosis
Group B streptococcal infection
Medicine
Health
Pediatrics

Newborn Screening Articles Winter[removed]_Clin_Chim_Acta._ 2012 Feb 18;[removed]):[removed]Epub 2011 Oct 29. The use of high resolution melting analysis to detect Fabry mutations in heterozygous females via dry bloodspot

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