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Predicate | Object |
---|---|
rdf:type | |
pubmed:issue |
2
|
pubmed:dateCreated |
1982-12-18
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:status |
MEDLINE
|
pubmed:issn |
0001-6527
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
23
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
239-45
|
pubmed:dateRevised |
2004-11-17
|
pubmed:meshHeading |
pubmed-meshheading:7136605-Chromosome Deletion,
pubmed-meshheading:7136605-Chromosomes, Human, 6-12 and X,
pubmed-meshheading:7136605-Craniofacial Dysostosis,
pubmed-meshheading:7136605-Female,
pubmed-meshheading:7136605-Hand Deformities, Congenital,
pubmed-meshheading:7136605-Heart Septal Defects, Ventricular,
pubmed-meshheading:7136605-Humans,
pubmed-meshheading:7136605-Infant, Newborn,
pubmed-meshheading:7136605-Karyotyping,
pubmed-meshheading:7136605-Syndrome
|
pubmed:year |
1982
|
pubmed:articleTitle |
11q--syndrome.
|
pubmed:publicationType |
Journal Article,
Case Reports
|