16506277

Source:http://linkedlifedata.com/resource/pubmed/id/16506277

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Subject	Predicate	Object	Context
pubmed-article:16506277	rdf:type	pubmed:Citation	lld:pubmed
pubmed-article:16506277	lifeskim:mentions	umls-concept:C0796366	lld:lifeskim
pubmed-article:16506277	lifeskim:mentions	umls-concept:C0033053	lld:lifeskim
pubmed-article:16506277	lifeskim:mentions	umls-concept:C1442161	lld:lifeskim
pubmed-article:16506277	lifeskim:mentions	umls-concept:C0205088	lld:lifeskim
pubmed-article:16506277	lifeskim:mentions	umls-concept:C1515568	lld:lifeskim
pubmed-article:16506277	pubmed:issue	3	lld:pubmed
pubmed-article:16506277	pubmed:dateCreated	2006-3-6	lld:pubmed
pubmed-article:16506277	pubmed:abstractText	To describe the prenatal phenotype of the 11q deletion syndrome (Jacobsen syndrome) and present the molecular characterization of the deletion in the case presented.	lld:pubmed
pubmed-article:16506277	pubmed:language	eng	lld:pubmed
pubmed-article:16506277	pubmed:journal	http://linkedlifedata.com/r...	lld:pubmed
pubmed-article:16506277	pubmed:citationSubset	IM	lld:pubmed
pubmed-article:16506277	pubmed:status	MEDLINE	lld:pubmed
pubmed-article:16506277	pubmed:month	Mar	lld:pubmed
pubmed-article:16506277	pubmed:issn	0197-3851	lld:pubmed
pubmed-article:16506277	pubmed:author	pubmed-author:SchubertCC	lld:pubmed
pubmed-article:16506277	pubmed:author	pubmed-author:HeroldSS	lld:pubmed
pubmed-article:16506277	pubmed:author	pubmed-author:ZollBB	lld:pubmed
pubmed-article:16506277	pubmed:author	pubmed-author:MännerJJ	lld:pubmed
pubmed-article:16506277	pubmed:author	pubmed-author:BurfeindPP	lld:pubmed
pubmed-article:16506277	pubmed:author	pubmed-author:BartelsII	lld:pubmed
pubmed-article:16506277	pubmed:author	pubmed-author:BoehmDD	lld:pubmed
pubmed-article:16506277	pubmed:author	pubmed-author:LacconeFF	lld:pubmed
pubmed-article:16506277	pubmed:author	pubmed-author:PauerH UHU	lld:pubmed
pubmed-article:16506277	pubmed:copyrightInfo	2006 John Wiley & Sons, Ltd.	lld:pubmed
pubmed-article:16506277	pubmed:issnType	Print	lld:pubmed
pubmed-article:16506277	pubmed:volume	26	lld:pubmed
pubmed-article:16506277	pubmed:owner	NLM	lld:pubmed
pubmed-article:16506277	pubmed:authorsComplete	Y	lld:pubmed
pubmed-article:16506277	pubmed:pagination	286-90	lld:pubmed
pubmed-article:16506277	pubmed:meshHeading	pubmed-meshheading:16506277...	lld:pubmed
pubmed-article:16506277	pubmed:meshHeading	pubmed-meshheading:16506277...	lld:pubmed
pubmed-article:16506277	pubmed:meshHeading	pubmed-meshheading:16506277...	lld:pubmed
pubmed-article:16506277	pubmed:meshHeading	pubmed-meshheading:16506277...	lld:pubmed
pubmed-article:16506277	pubmed:meshHeading	pubmed-meshheading:16506277...	lld:pubmed
pubmed-article:16506277	pubmed:meshHeading	pubmed-meshheading:16506277...	lld:pubmed
pubmed-article:16506277	pubmed:meshHeading	pubmed-meshheading:16506277...	lld:pubmed
pubmed-article:16506277	pubmed:meshHeading	pubmed-meshheading:16506277...	lld:pubmed
pubmed-article:16506277	pubmed:meshHeading	pubmed-meshheading:16506277...	lld:pubmed
pubmed-article:16506277	pubmed:meshHeading	pubmed-meshheading:16506277...	lld:pubmed
pubmed-article:16506277	pubmed:meshHeading	pubmed-meshheading:16506277...	lld:pubmed
pubmed-article:16506277	pubmed:year	2006	lld:pubmed
pubmed-article:16506277	pubmed:articleTitle	Prenatal diagnosis of a large de novo terminal deletion of chromosome 11q.	lld:pubmed
pubmed-article:16506277	pubmed:affiliation	Institute of Human Genetics, University of Goettingen, Goettingen, Germany.	lld:pubmed
pubmed-article:16506277	pubmed:publicationType	Journal Article	lld:pubmed
pubmed-article:16506277	pubmed:publicationType	Case Reports	lld:pubmed
http://linkedlifedata.com/r...	pubmed:referesTo	pubmed-article:16506277	lld:pubmed