reference/26052641

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/26052641

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publicationName	Journal of Medical Screening
startingPage	132
bibliographicCitation	Zekanowski C, Nowacka M, Radomyska B, Cabalska B. Should newborn mutation scanning for hyperphenylalaninaemia and galactosaemia be implemented? A Polish experience. J Med Screen. 2001;8(3):132–6. doi: 10.1136/jms.8.3.132. PMID: 11678552.
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date	2001-09-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://doi.org/10.1136/jms.8.3.132 https://pubmed.ncbi.nlm.nih.gov/11678552
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language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	Should newborn mutation scanning for hyperphenylalaninaemia and galactosaemia be implemented? A Polish experience
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