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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
4
|
| pubmed:dateCreated |
1989-3-16
|
| pubmed:abstractText |
This report describes a child with the Klippel-Feil anomaly and sacral agenesis. A review of the literature revealed that this association has been recorded on other occasions. We believe that this combination of findings is significant and thus propose to call this the Klippel-Feil anomaly type IV.
|
| pubmed:commentsCorrections | |
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:status |
MEDLINE
|
| pubmed:issn |
0270-4145
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:volume |
8
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
297-301
|
| pubmed:dateRevised |
2005-11-16
|
| pubmed:meshHeading | |
| pubmed:year |
1988
|
| pubmed:articleTitle |
Klippel-Feil anomaly with sacral agenesis: an additional subtype, type IV.
|
| pubmed:affiliation |
Department of Pediatrics B, Beilinson Medical Center, Tel Hashomer, Israel.
|
| pubmed:publicationType |
Journal Article,
Review,
Case Reports
|