6978128

Source:http://linkedlifedata.com/resource/pubmed/id/6978128

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0005745, umls-concept:C0013581, umls-concept:C0271183, umls-concept:C0439660
pubmed:issue	2
pubmed:dateCreated	1982-5-21
pubmed:abstractText	A previously undescribed syndrome of bilateral blepharoptosis, ectopia lentis, and high myopia apparently was dominantly inherited and originated from a spontaneous genetic mutation. The syndrome seems to be caused by a decrease in the tensile strength of the levator aponeurosis, the zonules, and the sclera.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/7706534
pubmed:citationSubset	AIM
pubmed:status	MEDLINE
pubmed:month	Feb
pubmed:issn	0003-9950
pubmed:author	pubmed-author:AndersonR LRL, pubmed-author:GillumW NWN
pubmed:issnType	Print
pubmed:volume	100
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	282-4
pubmed:dateRevised	2004-11-17
pubmed:meshHeading	pubmed-meshheading:6978128-Adolescent, pubmed-meshheading:6978128-Adult, pubmed-meshheading:6978128-Aged, pubmed-meshheading:6978128-Blepharoptosis, pubmed-meshheading:6978128-Cataract, pubmed-meshheading:6978128-Child, pubmed-meshheading:6978128-Child, Preschool, pubmed-meshheading:6978128-Ectopia Lentis, pubmed-meshheading:6978128-Endophthalmitis, pubmed-meshheading:6978128-Female, pubmed-meshheading:6978128-Genes, Dominant, pubmed-meshheading:6978128-Humans, pubmed-meshheading:6978128-Infant, pubmed-meshheading:6978128-Lens Subluxation, pubmed-meshheading:6978128-Male, pubmed-meshheading:6978128-Middle Aged, pubmed-meshheading:6978128-Mutation, pubmed-meshheading:6978128-Myopia, pubmed-meshheading:6978128-Syndrome
pubmed:year	1982
pubmed:articleTitle	Dominantly inherited blepharoptosis, high myopia, and ectopia lentis.
pubmed:publicationType	Journal Article, Case Reports