14619632

Source:http://linkedlifedata.com/resource/pubmed/id/14619632

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0013936, umls-concept:C0014876, umls-concept:C0022077, umls-concept:C0679316, umls-concept:C1457869
pubmed:issue	289
pubmed:dateCreated	2003-11-17
pubmed:abstractText	We present an infant with heterochromia of the irides and a motility disorder of the oesophagus. The association between Hirschsprung's disease and heterochromia of the irides has been reported in the past and has been explained by the common origin during embryogenesis of the parasympathetic ganglion cells and the stroma of the iris.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/7505353
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:issn	0081-0746
pubmed:author	pubmed-author:CasteelsII, pubmed-author:DevriendtKK, pubmed-author:GoethalsSS, pubmed-author:HoffmanII
pubmed:issnType	Print
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	73-7
pubmed:dateRevised	2004-11-17
pubmed:meshHeading	pubmed-meshheading:14619632-Child, Preschool, pubmed-meshheading:14619632-Esophageal Motility Disorders, pubmed-meshheading:14619632-Esophagitis, pubmed-meshheading:14619632-Female, pubmed-meshheading:14619632-Humans, pubmed-meshheading:14619632-Iris
pubmed:year	2003
pubmed:articleTitle	Heterochromia of the irides and a motility disorder of the oesophagus: a coincidence or a defect during embryogenesis?
pubmed:affiliation	Dept. of Ophthalmology, University Hospital St. Raphaël, Kapucijnenvoer 33, B-3000 Leuven, Belgium.
pubmed:publicationType	Journal Article, Case Reports