491337

Source:http://linkedlifedata.com/resource/pubmed/id/491337

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0008625, umls-concept:C0039082, umls-concept:C0265490, umls-concept:C0432412, umls-concept:C0596790, umls-concept:C0678226, umls-concept:C1140618, umls-concept:C1297882, umls-concept:C1442161
pubmed:issue	4
pubmed:dateCreated	1979-12-27
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0072456
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:month	Oct
pubmed:issn	0021-7263
pubmed:author	pubmed-author:LeonardC OCO, pubmed-author:PaiG SGS, pubmed-author:PyeritzR ERE, pubmed-author:ThomasG HGH, pubmed-author:ValleD LDL, pubmed-author:WardJ CJC
pubmed:issnType	Print
pubmed:volume	145
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	162-9
pubmed:dateRevised	2011-11-17
pubmed:meshHeading	pubmed-meshheading:491337-Abnormalities, Multiple, pubmed-meshheading:491337-Adult, pubmed-meshheading:491337-Chromosome Aberrations, pubmed-meshheading:491337-Chromosome Deletion, pubmed-meshheading:491337-Chromosome Disorders, pubmed-meshheading:491337-Chromosome Mapping, pubmed-meshheading:491337-Chromosomes, Human, 21-22 and Y, pubmed-meshheading:491337-Chromosomes, Human, 6-12 and X, pubmed-meshheading:491337-Female, pubmed-meshheading:491337-Growth Disorders, pubmed-meshheading:491337-Humans, pubmed-meshheading:491337-Infant, pubmed-meshheading:491337-Intellectual Disability, pubmed-meshheading:491337-Male, pubmed-meshheading:491337-Syndrome, pubmed-meshheading:491337-Trisomy
pubmed:year	1979
pubmed:articleTitle	Syndromes due to chromosomal abnormalities: partial trisomy 22, interstitial deletion of the long arm of 13, and trisomy 8.
pubmed:publicationType	Journal Article, Research Support, U.S. Gov't, P.H.S., Case Reports