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Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
|
pubmed:dateCreated |
1981-3-27
|
pubmed:language |
fre
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Apr
|
pubmed:issn |
0041-6959
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
109
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
591-5
|
pubmed:dateRevised |
2009-11-11
|
pubmed:meshHeading |
pubmed-meshheading:7456152-Congenital Hypothyroidism,
pubmed-meshheading:7456152-Humans,
pubmed-meshheading:7456152-Infant, Newborn,
pubmed-meshheading:7456152-Mass Screening,
pubmed-meshheading:7456152-Metabolism, Inborn Errors,
pubmed-meshheading:7456152-Phenylketonurias,
pubmed-meshheading:7456152-Quebec,
pubmed-meshheading:7456152-Tyrosine
|
pubmed:year |
1980
|
pubmed:articleTitle |
[Hereditary metabolic diseases in Quebec: blood screening].
|
pubmed:publicationType |
Journal Article,
English Abstract
|