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Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3B
|
pubmed:dateCreated |
1983-1-27
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:status |
MEDLINE
|
pubmed:issn |
0547-6844
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
18
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
237-42
|
pubmed:dateRevised |
2011-11-17
|
pubmed:meshHeading |
pubmed-meshheading:7139108-Child,
pubmed-meshheading:7139108-Epilepsy,
pubmed-meshheading:7139108-Female,
pubmed-meshheading:7139108-Genes, Recessive,
pubmed-meshheading:7139108-Humans,
pubmed-meshheading:7139108-Intellectual Disability,
pubmed-meshheading:7139108-Male,
pubmed-meshheading:7139108-Nose,
pubmed-meshheading:7139108-Pedigree,
pubmed-meshheading:7139108-Syndrome
|
pubmed:year |
1982
|
pubmed:articleTitle |
Syndrome of psychomotor retardation, bulbous nose, and epilepsy.
|
pubmed:publicationType |
Journal Article,
Case Reports
|