Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
5
pubmed:dateCreated
1972-7-29
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
May
pubmed:issn
0002-9394
pubmed:author
pubmed:issnType
Print
pubmed:volume
73
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
718-41
pubmed:dateRevised
2004-11-17
pubmed:meshHeading
pubmed-meshheading:4260446-Carbohydrate Metabolism, Inborn Errors, pubmed-meshheading:4260446-Child, pubmed-meshheading:4260446-Cornea, pubmed-meshheading:4260446-Corneal Opacity, pubmed-meshheading:4260446-Craniofacial Dysostosis, pubmed-meshheading:4260446-Cytoplasm, pubmed-meshheading:4260446-Dwarfism, pubmed-meshheading:4260446-Eye, pubmed-meshheading:4260446-Eye Diseases, pubmed-meshheading:4260446-Glycosaminoglycans, pubmed-meshheading:4260446-Histocytochemistry, pubmed-meshheading:4260446-Histological Techniques, pubmed-meshheading:4260446-Humans, pubmed-meshheading:4260446-Intracranial Pressure, pubmed-meshheading:4260446-Male, pubmed-meshheading:4260446-Microscopy, Electron, pubmed-meshheading:4260446-Optic Atrophy, pubmed-meshheading:4260446-Retina, pubmed-meshheading:4260446-Sclera, pubmed-meshheading:4260446-Uvea
pubmed:year
1972
pubmed:articleTitle
Ocular pathology of the Maroteaux-Lamy syndrome (systemic mucopolysaccharidosis type VI). Histologic and ultrastructural report of two cases.
pubmed:publicationType
Journal Article