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Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
|
pubmed:dateCreated |
1977-7-29
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:status |
MEDLINE
|
pubmed:issn |
0301-0171
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
18
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
108
|
pubmed:dateRevised |
2006-11-15
|
pubmed:meshHeading |
pubmed-meshheading:862431-Abnormalities, Multiple,
pubmed-meshheading:862431-Chromosome Aberrations,
pubmed-meshheading:862431-Chromosome Deletion,
pubmed-meshheading:862431-Chromosomes, Human, 1-3,
pubmed-meshheading:862431-Humans,
pubmed-meshheading:862431-Infant, Newborn,
pubmed-meshheading:862431-Male
|
pubmed:year |
1977
|
pubmed:articleTitle |
Deletion of the short arm of chromosome 2 from a subject with congenital anomalies. Repository identification no. GM-1138.
|
pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Case Reports
|