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Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
|
pubmed:dateCreated |
1983-4-21
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:status |
MEDLINE
|
pubmed:month |
Sep
|
pubmed:issn |
0021-5074
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
27
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
283-8
|
pubmed:dateRevised |
2011-11-17
|
pubmed:meshHeading |
pubmed-meshheading:7161937-Chromosomes, Human, 13-15,
pubmed-meshheading:7161937-Chromosomes, Human, 6-12 and X,
pubmed-meshheading:7161937-Dermatoglyphics,
pubmed-meshheading:7161937-Female,
pubmed-meshheading:7161937-Growth Disorders,
pubmed-meshheading:7161937-Humans,
pubmed-meshheading:7161937-Infant,
pubmed-meshheading:7161937-Intellectual Disability,
pubmed-meshheading:7161937-Trisomy
|
pubmed:year |
1982
|
pubmed:articleTitle |
A case of partial 14 trisomy, 47,XX, + der(14),t(9p + ;14q-).
|
pubmed:publicationType |
Journal Article,
Case Reports
|