690768

Source:http://linkedlifedata.com/resource/pubmed/id/690768

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0014544, umls-concept:C0221033, umls-concept:C0332281, umls-concept:C1859420
pubmed:issue	3
pubmed:dateCreated	1978-11-18
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0375410
pubmed:citationSubset	AIM
pubmed:status	MEDLINE
pubmed:month	Sep
pubmed:issn	0022-3476
pubmed:author	pubmed-author:BarclayG RGR, pubmed-author:BrownJ KJK, pubmed-author:GraceEE, pubmed-author:SillsJ AJA, pubmed-author:UrbaniakS JSJ, pubmed-author:WoodS MSM
pubmed:issnType	Print
pubmed:volume	93
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	469-71
pubmed:dateRevised	2004-11-17
pubmed:meshHeading	pubmed-meshheading:690768-Adolescent, pubmed-meshheading:690768-Agammaglobulinemia, pubmed-meshheading:690768-Child, pubmed-meshheading:690768-Epilepsy, Temporal Lobe, pubmed-meshheading:690768-Female, pubmed-meshheading:690768-Humans, pubmed-meshheading:690768-Sex Chromosome Aberrations, pubmed-meshheading:690768-Sex Chromosomes, pubmed-meshheading:690768-X Chromosome
pubmed:year	1978
pubmed:articleTitle	XXX syndrome associated with immunoglobulin deficiency and epilepsy.
pubmed:publicationType	Journal Article, Case Reports