18387282

Source:http://linkedlifedata.com/resource/pubmed/id/18387282

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0019904, umls-concept:C0026882, umls-concept:C0079301, umls-concept:C0205197, umls-concept:C0205314, umls-concept:C0301630, umls-concept:C0678227, umls-concept:C0679622, umls-concept:C1416783, umls-concept:C1858460
pubmed:issue	1
pubmed:dateCreated	2008-5-7
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9011485
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Cell Adhesion Molecules, http://linkedlifedata.com/resource/pubmed/chemical/kalinin
pubmed:status	MEDLINE
pubmed:month	Jul
pubmed:issn	0923-1811
pubmed:author	pubmed-author:CastigliaDanieleD, pubmed-author:CastoriMarcoM, pubmed-author:CovaciuClaudiaC, pubmed-author:FloriddiaGiovannaG, pubmed-author:ParadisiMauroM, pubmed-author:PisaneschiElisaE, pubmed-author:TorrenteIsabellaI
pubmed:issnType	Print
pubmed:volume	51
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	58-61
pubmed:meshHeading	pubmed-meshheading:18387282-Adult, pubmed-meshheading:18387282-Cell Adhesion Molecules, pubmed-meshheading:18387282-Epidermolysis Bullosa, Junctional, pubmed-meshheading:18387282-Female, pubmed-meshheading:18387282-Homozygote, pubmed-meshheading:18387282-Humans, pubmed-meshheading:18387282-Infant, pubmed-meshheading:18387282-Male, pubmed-meshheading:18387282-Mutation, Missense, pubmed-meshheading:18387282-Uniparental Disomy
pubmed:year	2008
pubmed:articleTitle	Complete maternal isodisomy causing reduction to homozygosity for a novel LAMB3 mutation in Herlitz junctional epidermolysis bullosa.
pubmed:publicationType	Letter, Case Reports, Research Support, Non-U.S. Gov't