9818897

Source:http://linkedlifedata.com/resource/pubmed/id/9818897

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0008665, umls-concept:C0039082, umls-concept:C0266464
pubmed:issue	5
pubmed:dateCreated	1998-12-3
pubmed:abstractText	We report two children with chromosome 22q11 deletion syndrome who had neuroradiologic evidence of polymicrogyria. The diagnosis of chromosome 22q11 deletion should be considered in individuals with polymicrogyria.
pubmed:grant	http://linkedlifedata.com/resource/pubmed/grant/NS01773
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0401060
pubmed:citationSubset	AIM
pubmed:status	MEDLINE
pubmed:month	Nov
pubmed:issn	0028-3878
pubmed:author	pubmed-author:BinghamP MPM, pubmed-author:LynchDD, pubmed-author:McDonald-McGinnDD, pubmed-author:ZackaiEE
pubmed:issnType	Print
pubmed:volume	51
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	1500-2
pubmed:dateRevised	2007-11-15
pubmed:meshHeading	pubmed-meshheading:9818897-Brain, pubmed-meshheading:9818897-Brain Stem, pubmed-meshheading:9818897-Child, Preschool, pubmed-meshheading:9818897-Chromosome Deletion, pubmed-meshheading:9818897-Chromosome Mapping, pubmed-meshheading:9818897-Chromosomes, Human, Pair 22, pubmed-meshheading:9818897-Congenital Abnormalities, pubmed-meshheading:9818897-Electroencephalography, pubmed-meshheading:9818897-Evoked Potentials, Auditory, pubmed-meshheading:9818897-Humans, pubmed-meshheading:9818897-Male, pubmed-meshheading:9818897-Syndrome
pubmed:year	1998
pubmed:articleTitle	Polymicrogyria in chromosome 22 delection syndrome.
pubmed:affiliation	Division of Neurology, Children's Hospital of Philadelphia, PA 19104, USA.
pubmed:publicationType	Journal Article, Research Support, U.S. Gov't, P.H.S., Case Reports