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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
2
|
| pubmed:dateCreated |
1979-5-16
|
| pubmed:abstractText |
A new case of familial Caffey's disease is referred with focused clinic, radiologic and anatopathologic aspects. The hereditary patterns may obey a autosomic dominant one, with variable penetrance and expressivity. Thus a improved familial research is necessary in all the infantile cortical hyperostosis cases.
|
| pubmed:language |
spa
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:status |
MEDLINE
|
| pubmed:month |
Feb
|
| pubmed:issn |
0302-4342
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:volume |
12
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
155-8
|
| pubmed:dateRevised |
2006-11-15
|
| pubmed:meshHeading | |
| pubmed:year |
1979
|
| pubmed:articleTitle |
[Familial infantile cortical hyperostosis (author's transl)].
|
| pubmed:publicationType |
Journal Article,
English Abstract,
Case Reports
|