Switch to
| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
2
|
| pubmed:dateCreated |
1973-2-2
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
AIM
|
| pubmed:status |
MEDLINE
|
| pubmed:month |
Jan
|
| pubmed:issn |
0028-4793
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:day |
11
|
| pubmed:volume |
288
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
106-7
|
| pubmed:dateRevised |
2004-11-17
|
| pubmed:meshHeading |
pubmed-meshheading:4629273-Female,
pubmed-meshheading:4629273-Heterozygote,
pubmed-meshheading:4629273-Humans,
pubmed-meshheading:4629273-Infant,
pubmed-meshheading:4629273-Karyotyping,
pubmed-meshheading:4629273-Mucopolysaccharidosis II,
pubmed-meshheading:4629273-Retinitis Pigmentosa,
pubmed-meshheading:4629273-Sex Chromosomes
|
| pubmed:year |
1973
|
| pubmed:articleTitle |
The Hunter syndrome in a 46 XX girl.
|
| pubmed:publicationType |
Journal Article
|