11678552

Source:http://linkedlifedata.com/resource/pubmed/id/11678552

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Subject	Predicate	Object	Context
pubmed-article:11678552	rdf:type	pubmed:Citation	lld:pubmed
pubmed-article:11678552	lifeskim:mentions	umls-concept:C0021289	lld:lifeskim
pubmed-article:11678552	lifeskim:mentions	umls-concept:C0220896	lld:lifeskim
pubmed-article:11678552	lifeskim:mentions	umls-concept:C0026882	lld:lifeskim
pubmed-article:11678552	lifeskim:mentions	umls-concept:C0016952	lld:lifeskim
pubmed-article:11678552	lifeskim:mentions	umls-concept:C0751435	lld:lifeskim
pubmed-article:11678552	lifeskim:mentions	umls-concept:C0596545	lld:lifeskim
pubmed-article:11678552	lifeskim:mentions	umls-concept:C0441633	lld:lifeskim
pubmed-article:11678552	pubmed:issue	3	lld:pubmed
pubmed-article:11678552	pubmed:dateCreated	2001-10-25	lld:pubmed
pubmed-article:11678552	pubmed:abstractText	To elucidate whether screening for mutations causing hyperphenylalaninaemia (HPA) and classic galactosaemia could provide important, additional information on a clinical phenotype.	lld:pubmed
pubmed-article:11678552	pubmed:language	eng	lld:pubmed
pubmed-article:11678552	pubmed:journal	http://linkedlifedata.com/r...	lld:pubmed
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pubmed-article:11678552	pubmed:status	MEDLINE	lld:pubmed
pubmed-article:11678552	pubmed:issn	0969-1413	lld:pubmed
pubmed-article:11678552	pubmed:author	pubmed-author:NowackaMM	lld:pubmed
pubmed-article:11678552	pubmed:author	pubmed-author:CabalskaBB	lld:pubmed
pubmed-article:11678552	pubmed:author	pubmed-author:ZekanowskiCC	lld:pubmed
pubmed-article:11678552	pubmed:author	pubmed-author:RadomyskaBB	lld:pubmed
pubmed-article:11678552	pubmed:issnType	Print	lld:pubmed
pubmed-article:11678552	pubmed:volume	8	lld:pubmed
pubmed-article:11678552	pubmed:owner	NLM	lld:pubmed
pubmed-article:11678552	pubmed:authorsComplete	Y	lld:pubmed
pubmed-article:11678552	pubmed:pagination	132-6	lld:pubmed
pubmed-article:11678552	pubmed:dateRevised	2004-11-17	lld:pubmed
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pubmed-article:11678552	pubmed:meshHeading	pubmed-meshheading:11678552...	lld:pubmed
pubmed-article:11678552	pubmed:year	2001	lld:pubmed
pubmed-article:11678552	pubmed:articleTitle	Should newborn mutation scanning for hyperphenylalaninaemia and galactosaemia be implemented? A Polish experience.	lld:pubmed
pubmed-article:11678552	pubmed:affiliation	Department of Medical Genetics, National Research Institute of Mother and Child, Warszawa, Poland. czarekz@iimcb.gov.pl	lld:pubmed
pubmed-article:11678552	pubmed:publicationType	Journal Article	lld:pubmed
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