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Neonatal hypothyroidism, phenylketonuria and galactosemia screening in metropolitan Shanghai



Neonatal hypothyroidism, phenylketonuria and galactosemia screening in metropolitan Shanghai



Chinese Medical Journal 97(1): 61-65



Neonatal screening for inborn errors of metabolism and congenital hypothyroidism has received increasing attention in recent years, because early detection and treatment can prevent permanent brain damage or death of the affected child. Experience in screening for inborn errors of metabolism, congenital hypothyroidism, phenylketonuria and galactosemia in 31,861 newborns from Oct. 1981 to Sept. 1982 is described.

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Accession: 001414893

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PMID: 6428834


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