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Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
|
pubmed:dateCreated |
1982-3-13
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:status |
MEDLINE
|
pubmed:month |
Apr
|
pubmed:issn |
0020-7292
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
19
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
103-7
|
pubmed:dateRevised |
2004-11-17
|
pubmed:meshHeading |
pubmed-meshheading:6119240-Abnormalities, Multiple,
pubmed-meshheading:6119240-Adult,
pubmed-meshheading:6119240-Chromosomes, Human, 6-12 and X,
pubmed-meshheading:6119240-Female,
pubmed-meshheading:6119240-Humans,
pubmed-meshheading:6119240-Karyotyping,
pubmed-meshheading:6119240-Male,
pubmed-meshheading:6119240-Syndrome,
pubmed-meshheading:6119240-Translocation, Genetic,
pubmed-meshheading:6119240-Trisomy
|
pubmed:year |
1981
|
pubmed:articleTitle |
Partial trisomy 10q syndrome. Report of a case with new findings.
|
pubmed:publicationType |
Journal Article,
Case Reports
|