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Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
|
pubmed:dateCreated |
1978-1-27
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:status |
MEDLINE
|
pubmed:month |
Nov
|
pubmed:issn |
0340-6717
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:day |
2
|
pubmed:volume |
39
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
109-12
|
pubmed:dateRevised |
2004-11-17
|
pubmed:meshHeading |
pubmed-meshheading:924437-Adult,
pubmed-meshheading:924437-Chromosomes, Human, 4-5,
pubmed-meshheading:924437-Cri-du-Chat Syndrome,
pubmed-meshheading:924437-Female,
pubmed-meshheading:924437-Humans,
pubmed-meshheading:924437-Infant,
pubmed-meshheading:924437-Karyotyping,
pubmed-meshheading:924437-Male,
pubmed-meshheading:924437-Translocation, Genetic
|
pubmed:year |
1977
|
pubmed:articleTitle |
Cri-Du-Chat syndrome in a child with a 46,XX,der(5),t(4;5)(q32;p14)pat Karyotype.
|
pubmed:publicationType |
Journal Article
|