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Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2-3
|
pubmed:dateCreated |
1980-1-28
|
pubmed:language |
fre
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:status |
MEDLINE
|
pubmed:issn |
0300-984X
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
49-50
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
134-66
|
pubmed:dateRevised |
2011-11-17
|
pubmed:meshHeading |
pubmed-meshheading:1053152-Abnormalities, Multiple,
pubmed-meshheading:1053152-Chromosomes, Human, 21-22 and Y,
pubmed-meshheading:1053152-Female,
pubmed-meshheading:1053152-Heart Defects, Congenital,
pubmed-meshheading:1053152-Humans,
pubmed-meshheading:1053152-Infant, Newborn,
pubmed-meshheading:1053152-Intellectual Disability,
pubmed-meshheading:1053152-Male,
pubmed-meshheading:1053152-Trisomy
|
pubmed:articleTitle |
[Trisomy 22].
|
pubmed:publicationType |
Journal Article
|