Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
11
pubmed:dateCreated
1999-11-23
pubmed:abstractText
To undertake a clinical and molecular analysis of a previously unpublished kindred with a phenotypically distinct vitreoretinopathy characterized by associated ocular developmental abnormalities.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Nov
pubmed:issn
0161-6420
pubmed:author
pubmed:issnType
Print
pubmed:volume
106
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
2074-81
pubmed:dateRevised
2010-11-18
pubmed:meshHeading
pubmed-meshheading:10571340-Abnormalities, Multiple, pubmed-meshheading:10571340-Adolescent, pubmed-meshheading:10571340-Adult, pubmed-meshheading:10571340-Aged, pubmed-meshheading:10571340-Child, pubmed-meshheading:10571340-Chromosome Mapping, pubmed-meshheading:10571340-Chromosomes, Human, Pair 5, pubmed-meshheading:10571340-DNA, pubmed-meshheading:10571340-Eye Abnormalities, pubmed-meshheading:10571340-Eye Diseases, Hereditary, pubmed-meshheading:10571340-Female, pubmed-meshheading:10571340-Genetic Linkage, pubmed-meshheading:10571340-Genotype, pubmed-meshheading:10571340-Humans, pubmed-meshheading:10571340-Male, pubmed-meshheading:10571340-Middle Aged, pubmed-meshheading:10571340-Pedigree, pubmed-meshheading:10571340-Polymerase Chain Reaction, pubmed-meshheading:10571340-Retina, pubmed-meshheading:10571340-Vitreous Body
pubmed:year
1999
pubmed:articleTitle
A novel hereditary developmental vitreoretinopathy with multiple ocular abnormalities localizing to a 5-cM region of chromosome 5q13-q14.
pubmed:affiliation
University Department of Medical Genetics and Regional Genetic Service, St. Mary's Hospital, Manchester, England. gblack@fs1.cmht.nwest.nhs.uk
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't