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Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
|
pubmed:dateCreated |
1979-5-23
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
AIM
|
pubmed:status |
MEDLINE
|
pubmed:month |
Mar
|
pubmed:issn |
0002-922X
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
133
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
330
|
pubmed:dateRevised |
2004-11-17
|
pubmed:meshHeading |
pubmed-meshheading:154838-Diagnosis, Differential,
pubmed-meshheading:154838-Down Syndrome,
pubmed-meshheading:154838-Female,
pubmed-meshheading:154838-Humans,
pubmed-meshheading:154838-Infant, Newborn,
pubmed-meshheading:154838-Sex Chromosome Aberrations,
pubmed-meshheading:154838-Syndrome,
pubmed-meshheading:154838-X Chromosome
|
pubmed:year |
1979
|
pubmed:articleTitle |
The penta X (49,XXXXX) syndrome: danger of confusing phenotype with mongolism.
|
pubmed:publicationType |
Journal Article,
Case Reports
|