Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
4
pubmed:dateCreated
1999-4-28
pubmed:abstractText
Characterize the phenotype of autosomal dominant Stargardt-like macular dystrophy in two families linked to chromosome 6q14 and determine whether they share a common ancestry.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:status
MEDLINE
pubmed:month
Apr
pubmed:issn
0002-9394
pubmed:author
pubmed:issnType
Print
pubmed:volume
127
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
426-35
pubmed:dateRevised
2010-11-18
pubmed:meshHeading
pubmed-meshheading:10218695-Adolescent, pubmed-meshheading:10218695-Adult, pubmed-meshheading:10218695-Aged, pubmed-meshheading:10218695-Aged, 80 and over, pubmed-meshheading:10218695-Child, pubmed-meshheading:10218695-Chromosome Mapping, pubmed-meshheading:10218695-Chromosomes, Human, Pair 6, pubmed-meshheading:10218695-Female, pubmed-meshheading:10218695-Fluorescein Angiography, pubmed-meshheading:10218695-Follow-Up Studies, pubmed-meshheading:10218695-Fundus Oculi, pubmed-meshheading:10218695-Genetic Linkage, pubmed-meshheading:10218695-Genotype, pubmed-meshheading:10218695-Haplotypes, pubmed-meshheading:10218695-Humans, pubmed-meshheading:10218695-Macular Degeneration, pubmed-meshheading:10218695-Male, pubmed-meshheading:10218695-Middle Aged, pubmed-meshheading:10218695-Pedigree, pubmed-meshheading:10218695-Phenotype, pubmed-meshheading:10218695-Vision Disorders, pubmed-meshheading:10218695-Visual Acuity
pubmed:year
1999
pubmed:articleTitle
Autosomal dominant Stargardt-like macular dystrophy: I. Clinical characterization, longitudinal follow-up, and evidence for a common ancestry in families linked to chromosome 6q14.
pubmed:affiliation
Casey Eye Institute, Department of Ophthalmology, Oregon Health Sciences University, Portland, USA.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't