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Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1013
|
pubmed:dateCreated |
1980-9-23
|
pubmed:language |
ita
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:status |
MEDLINE
|
pubmed:issn |
0031-2983
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
71
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
412-5
|
pubmed:dateRevised |
2004-11-17
|
pubmed:meshHeading |
pubmed-meshheading:162000-Chromosomes, Human, 1-3,
pubmed-meshheading:162000-Chromosomes, Human, 21-22 and Y,
pubmed-meshheading:162000-Down Syndrome,
pubmed-meshheading:162000-Humans,
pubmed-meshheading:162000-Infant,
pubmed-meshheading:162000-Infant, Newborn,
pubmed-meshheading:162000-Male,
pubmed-meshheading:162000-Translocation, Genetic,
pubmed-meshheading:162000-Trisomy
|
pubmed:articleTitle |
[Trisomy 21 due to segregation 3:1].
|
pubmed:publicationType |
Journal Article,
Case Reports
|