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Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
10
|
pubmed:dateCreated |
1977-8-12
|
pubmed:language |
ita
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:status |
MEDLINE
|
pubmed:month |
Mar
|
pubmed:issn |
0026-4946
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:day |
24
|
pubmed:volume |
29
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
667-72
|
pubmed:dateRevised |
2006-11-15
|
pubmed:meshHeading |
pubmed-meshheading:875934-Abnormalities, Multiple,
pubmed-meshheading:875934-Chromosome Aberrations,
pubmed-meshheading:875934-Dwarfism,
pubmed-meshheading:875934-Female,
pubmed-meshheading:875934-Humans,
pubmed-meshheading:875934-Infant, Newborn,
pubmed-meshheading:875934-Progeria,
pubmed-meshheading:875934-Syndrome
|
pubmed:year |
1977
|
pubmed:articleTitle |
[A case of leprechaunism with anomalous karyotype (46,XX/47,XX?r+)].
|
pubmed:publicationType |
Journal Article,
English Abstract,
Case Reports
|