Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
2000-1-14
pubmed:abstractText
Localization of the gene responsible for autosomal dominant atrophic macular degeneration (adMD) in a large pedigree UM:H785.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jan
pubmed:issn
0146-0404
pubmed:author
pubmed:issnType
Print
pubmed:volume
41
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
248-55
pubmed:dateRevised
2010-11-18
pubmed:meshHeading
pubmed-meshheading:10634627-Adolescent, pubmed-meshheading:10634627-Adult, pubmed-meshheading:10634627-Atrophy, pubmed-meshheading:10634627-Choroid Diseases, pubmed-meshheading:10634627-Chromosome Mapping, pubmed-meshheading:10634627-Chromosomes, Human, Pair 6, pubmed-meshheading:10634627-Electroretinography, pubmed-meshheading:10634627-Eye Proteins, pubmed-meshheading:10634627-Female, pubmed-meshheading:10634627-Fluorescein Angiography, pubmed-meshheading:10634627-Genetic Linkage, pubmed-meshheading:10634627-Genotype, pubmed-meshheading:10634627-Haplotypes, pubmed-meshheading:10634627-Humans, pubmed-meshheading:10634627-Macula Lutea, pubmed-meshheading:10634627-Macular Degeneration, pubmed-meshheading:10634627-Male, pubmed-meshheading:10634627-Middle Aged, pubmed-meshheading:10634627-Pedigree, pubmed-meshheading:10634627-Photoreceptor Cells, Vertebrate, pubmed-meshheading:10634627-Visual Acuity
pubmed:year
2000
pubmed:articleTitle
Autosomal dominant macular atrophy at 6q14 excludes CORD7 and MCDR1/PBCRA loci.
pubmed:affiliation
W.K. Kellogg Eye Center, University of Michigan, Ann Arbor 48105, USA.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't