19460271

Source:http://linkedlifedata.com/resource/pubmed/id/19460271

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Subject	Predicate	Object	Context
pubmed-article:19460271	rdf:type	pubmed:Citation	lld:pubmed
pubmed-article:19460271	lifeskim:mentions	umls-concept:C0029434	lld:lifeskim
pubmed-article:19460271	lifeskim:mentions	umls-concept:C2931264	lld:lifeskim
pubmed-article:19460271	lifeskim:mentions	umls-concept:C0039082	lld:lifeskim
pubmed-article:19460271	pubmed:issue	2	lld:pubmed
pubmed-article:19460271	pubmed:dateCreated	2009-5-22	lld:pubmed
pubmed-article:19460271	pubmed:abstractText	Bruck syndrome is characterised by osteogenesis imperfecta and arthrogryposis multiplex. In some patients, mutations in the lysyl hydroxylase 2 gene (PLOD2, 3q23-q24) have been demonstrated. A male newborn with Bruck syndrome is reported.	lld:pubmed
pubmed-article:19460271	pubmed:language	eng	lld:pubmed
pubmed-article:19460271	pubmed:journal	http://linkedlifedata.com/r...	lld:pubmed
pubmed-article:19460271	pubmed:citationSubset	IM	lld:pubmed
pubmed-article:19460271	pubmed:chemical	http://linkedlifedata.com/r...	lld:pubmed
pubmed-article:19460271	pubmed:chemical	http://linkedlifedata.com/r...	lld:pubmed
pubmed-article:19460271	pubmed:status	MEDLINE	lld:pubmed
pubmed-article:19460271	pubmed:month	Jun	lld:pubmed
pubmed-article:19460271	pubmed:issn	1465-3281	lld:pubmed
pubmed-article:19460271	pubmed:author	pubmed-author:OzcanKK	lld:pubmed
pubmed-article:19460271	pubmed:author	pubmed-author:SatarMM	lld:pubmed
pubmed-article:19460271	pubmed:author	pubmed-author:NarliNN	lld:pubmed
pubmed-article:19460271	pubmed:author	pubmed-author:Yapicio?luHH	lld:pubmed
pubmed-article:19460271	pubmed:author	pubmed-author:ArikanOO	lld:pubmed
pubmed-article:19460271	pubmed:author	pubmed-author:OzbekM HMH	lld:pubmed
pubmed-article:19460271	pubmed:issnType	Electronic	lld:pubmed
pubmed-article:19460271	pubmed:volume	29	lld:pubmed
pubmed-article:19460271	pubmed:owner	NLM	lld:pubmed
pubmed-article:19460271	pubmed:authorsComplete	Y	lld:pubmed
pubmed-article:19460271	pubmed:pagination	159-62	lld:pubmed
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pubmed-article:19460271	pubmed:meshHeading	pubmed-meshheading:19460271...	lld:pubmed
pubmed-article:19460271	pubmed:meshHeading	pubmed-meshheading:19460271...	lld:pubmed
pubmed-article:19460271	pubmed:year	2009	lld:pubmed
pubmed-article:19460271	pubmed:articleTitle	Bruck syndrome: osteogenesis imperfecta and arthrogryposis multiplex congenita.	lld:pubmed
pubmed-article:19460271	pubmed:affiliation	Division of Neonatology, Department of Pediatrics, Faculty of Medicine, Cukurova University, Adana, Turkey. yyhacer@hotmail.com	lld:pubmed
pubmed-article:19460271	pubmed:publicationType	Journal Article	lld:pubmed
pubmed-article:19460271	pubmed:publicationType	Case Reports	lld:pubmed