16199543

Source:http://linkedlifedata.com/resource/pubmed/id/16199543

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0032659, umls-concept:C0034975, umls-concept:C0035201, umls-concept:C1278208, umls-concept:C2827447
pubmed:issue	10
pubmed:dateCreated	2005-10-3
pubmed:abstractText	Neonatal screening for metabolic diseases, involving samples stored on filter paper (Guthrie spots), provides a potential resource for genetic epidemiological studies.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/2985087R
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/DNA Primers
pubmed:status	MEDLINE
pubmed:month	Oct
pubmed:issn	1468-6244
pubmed:author	pubmed-author:HanneliusUU, pubmed-author:KeroPP, pubmed-author:LindgrenC MCM, pubmed-author:MalmbergAA, pubmed-author:MelénEE, pubmed-author:von DobelnUU
pubmed:issnType	Electronic
pubmed:volume	42
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	e60
pubmed:dateRevised	2008-11-20
pubmed:meshHeading	pubmed-meshheading:16199543-Alleles, pubmed-meshheading:16199543-DNA Primers, pubmed-meshheading:16199543-Gene Deletion, pubmed-meshheading:16199543-Gene Frequency, pubmed-meshheading:16199543-Genetics, Population, pubmed-meshheading:16199543-Heterozygote, pubmed-meshheading:16199543-Humans, pubmed-meshheading:16199543-Infant, Newborn, pubmed-meshheading:16199543-Models, Genetic, pubmed-meshheading:16199543-Neonatal Screening, pubmed-meshheading:16199543-Phenylketonurias, pubmed-meshheading:16199543-Polymorphism, Single Nucleotide, pubmed-meshheading:16199543-Registries, pubmed-meshheading:16199543-Specimen Handling
pubmed:year	2005
pubmed:articleTitle	Phenylketonuria screening registry as a resource for population genetic studies.
pubmed:publicationType	Letter, Research Support, Non-U.S. Gov't