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Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
|
pubmed:dateCreated |
1969-9-22
|
pubmed:language |
ita
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:status |
MEDLINE
|
pubmed:month |
Jan
|
pubmed:issn |
0015-5578
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
17
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
47-56
|
pubmed:dateRevised |
2007-11-15
|
pubmed:meshHeading |
pubmed-meshheading:5732818-Chromosome Aberrations,
pubmed-meshheading:5732818-Chromosome Disorders,
pubmed-meshheading:5732818-Chromosomes, Human, 6-12 and X,
pubmed-meshheading:5732818-Congenital Abnormalities,
pubmed-meshheading:5732818-Female,
pubmed-meshheading:5732818-Humans,
pubmed-meshheading:5732818-Infant,
pubmed-meshheading:5732818-Karyotyping
|
pubmed:year |
1968
|
pubmed:articleTitle |
[Probable mosaic type "normal-trisomy 6-12-monosomy 6-12" in an underdeveloped girl with a slight malformation].
|
pubmed:publicationType |
Journal Article
|