Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
7593
|
pubmed:dateCreated |
1969-4-4
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
AIM
|
pubmed:status |
MEDLINE
|
pubmed:month |
Mar
|
pubmed:issn |
0140-6736
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:day |
8
|
pubmed:volume |
1
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
531
|
pubmed:dateRevised |
2004-11-17
|
pubmed:meshHeading |
pubmed-meshheading:4179603-Adolescent,
pubmed-meshheading:4179603-Chromosome Aberrations,
pubmed-meshheading:4179603-Chromosomes, Human, 16-18,
pubmed-meshheading:4179603-Female,
pubmed-meshheading:4179603-Humans,
pubmed-meshheading:4179603-Klinefelter Syndrome,
pubmed-meshheading:4179603-Leukocytes,
pubmed-meshheading:4179603-Male,
pubmed-meshheading:4179603-Pedigree
|
pubmed:year |
1969
|
pubmed:articleTitle |
A homozygous chromosomal variant.
|
pubmed:publicationType |
Journal Article
|