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Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
12
|
pubmed:dateCreated |
1985-1-28
|
pubmed:language |
ita
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:status |
MEDLINE
|
pubmed:month |
Jun
|
pubmed:issn |
0026-4946
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:day |
30
|
pubmed:volume |
36
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
645-51
|
pubmed:dateRevised |
2006-11-15
|
pubmed:meshHeading |
pubmed-meshheading:6513900-Chromosomes, Human, 13-15,
pubmed-meshheading:6513900-Ectromelia,
pubmed-meshheading:6513900-Humans,
pubmed-meshheading:6513900-Infant, Newborn,
pubmed-meshheading:6513900-Karyotyping,
pubmed-meshheading:6513900-Male,
pubmed-meshheading:6513900-Pedigree,
pubmed-meshheading:6513900-Translocation, Genetic
|
pubmed:year |
1984
|
pubmed:articleTitle |
[Sirenoid syndrome. Description of a case].
|
pubmed:publicationType |
Journal Article,
English Abstract,
Case Reports
|