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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
4
|
| pubmed:dateCreated |
1979-3-13
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:chemical | |
| pubmed:status |
MEDLINE
|
| pubmed:month |
Dec
|
| pubmed:issn |
0041-1345
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:volume |
10
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
753-5
|
| pubmed:dateRevised |
2010-11-18
|
| pubmed:meshHeading |
pubmed-meshheading:734746-Adrenocortical Hyperfunction,
pubmed-meshheading:734746-Chromosome Mapping,
pubmed-meshheading:734746-Genetic Linkage,
pubmed-meshheading:734746-HLA Antigens,
pubmed-meshheading:734746-Humans,
pubmed-meshheading:734746-Mixed Function Oxygenases,
pubmed-meshheading:734746-Recombination, Genetic
|
| pubmed:year |
1978
|
| pubmed:articleTitle |
Mapping of the 21-hydroxylase deficiency gene within the HLA linkage group.
|
| pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
|