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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
4
|
| pubmed:dateCreated |
1998-6-10
|
| pubmed:abstractText |
Linkage analysis was performed on a large Danish family to refine the position of RP18, the locus for autosomal dominant retinitis pigmentosa, mapped previously between D1S534 and D1S305 in chromosome 1p13-q21. We genotyped the family members for five microsatellite-type DNA polymorphisms and mapped RP18 between D1S422 and D1S2858 to a region of less than 2 cM. No obvious candidate gene has yet been assigned to the chromosomal interval defined here.
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:status |
MEDLINE
|
| pubmed:month |
Apr
|
| pubmed:issn |
0340-6717
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:volume |
102
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
493-4
|
| pubmed:dateRevised |
2006-11-15
|
| pubmed:meshHeading |
pubmed-meshheading:9600251-Adult,
pubmed-meshheading:9600251-Chromosomes, Human, Pair 1,
pubmed-meshheading:9600251-Female,
pubmed-meshheading:9600251-Genes, Dominant,
pubmed-meshheading:9600251-Humans,
pubmed-meshheading:9600251-Male,
pubmed-meshheading:9600251-Pedigree,
pubmed-meshheading:9600251-Restriction Mapping,
pubmed-meshheading:9600251-Retinitis Pigmentosa
|
| pubmed:year |
1998
|
| pubmed:articleTitle |
Refined genetic mapping of autosomal dominant retinitis pigmentosa locus RP18 reduces the critical region to 2 cM between D1S442 and D1S2858 on chromosome 1q.
|
| pubmed:affiliation |
Institut für Humangenetik, Universitäts-Krankenhaus Eppendorf, Hamburg, Germany.
|
| pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|