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Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
|
pubmed:dateCreated |
1970-3-14
|
pubmed:language |
fre
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:status |
MEDLINE
|
pubmed:month |
Sep
|
pubmed:issn |
0031-4021
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
22
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
723-4
|
pubmed:dateRevised |
2004-11-17
|
pubmed:meshHeading |
pubmed-meshheading:5621089-Acrocephalosyndactylia,
pubmed-meshheading:5621089-Chromosome Aberrations,
pubmed-meshheading:5621089-Chromosome Disorders,
pubmed-meshheading:5621089-Chromosomes, Human, 1-3,
pubmed-meshheading:5621089-Humans,
pubmed-meshheading:5621089-Infant, Newborn,
pubmed-meshheading:5621089-Male
|
pubmed:year |
1967
|
pubmed:articleTitle |
[Apert's syndrome (acrocephalosyndactylia). A case in a newborn infant associated with a structural anomaly of chromosome no. 3].
|
pubmed:publicationType |
Journal Article
|