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To undertake a clinical and molecular analysis of a previously unpublished kindred with a phenotypically distinct vitreoretinopathy characterized by associated ocular developmental abnormalities.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
|