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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
5
|
| pubmed:dateCreated |
1987-3-12
|
| pubmed:abstractText |
Aplasia cutis congenita is an uncommon disorder characterized by a patchy defect of the scalp and other areas of the skin of the newborn. Several familial cases have been reported, including a set of identical twin girls. The disease was unique in our patient, one monozygotic twin.
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:status |
MEDLINE
|
| pubmed:month |
Nov
|
| pubmed:issn |
0736-8046
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:volume |
3
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
403-5
|
| pubmed:dateRevised |
2009-3-3
|
| pubmed:meshHeading | |
| pubmed:year |
1986
|
| pubmed:articleTitle |
Aplasia cutis congenita in one of monozygotic twins.
|
| pubmed:publicationType |
Journal Article,
Case Reports
|