11182677

Source:http://linkedlifedata.com/resource/pubmed/id/11182677

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0221912, umls-concept:C0265237, umls-concept:C0684224, umls-concept:C1533148
pubmed:issue	1
pubmed:dateCreated	2001-2-22
pubmed:abstractText	Blepharophimosis-ptosis-epicanthus inversus syndrome (BPES) is a rare inherited disorder with characteristic oculofacial affection of the eyelid region. Recent results of genetic analysis of the causative gene, as well as a hitherto unknown association with hormone-dependent endometrial carcinoma, motivated us to review this syndrome.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9710011
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:month	Feb
pubmed:issn	1091-8531
pubmed:author	pubmed-author:AbeckDD, pubmed-author:MöhrenschlagerMM, pubmed-author:RingJJ, pubmed-author:WessnerD BDB
pubmed:issnType	Print
pubmed:volume	5
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	58-9
pubmed:dateRevised	2006-4-21
pubmed:meshHeading	pubmed-meshheading:11182677-Blepharophimosis, pubmed-meshheading:11182677-Blepharoptosis, pubmed-meshheading:11182677-Child, pubmed-meshheading:11182677-Eye Abnormalities, pubmed-meshheading:11182677-Eyelids, pubmed-meshheading:11182677-Female, pubmed-meshheading:11182677-Humans, pubmed-meshheading:11182677-Skin Diseases, pubmed-meshheading:11182677-Syndrome
pubmed:year	2001
pubmed:articleTitle	Cutaneous peculiarities in blepharophimosis-ptosis-epicanthus inversus syndrome: report of a case.
pubmed:affiliation	Department of Dermatology and Allergy Biederstein, Technical University of Munich, Germany.
pubmed:publicationType	Journal Article, Case Reports