| pubmed-article:12359607 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:12359607 | lifeskim:mentions | umls-concept:C0035334 | lld:lifeskim |
| pubmed-article:12359607 | lifeskim:mentions | umls-concept:C0596142 | lld:lifeskim |
| pubmed-article:12359607 | lifeskim:mentions | umls-concept:C0026882 | lld:lifeskim |
| pubmed-article:12359607 | lifeskim:mentions | umls-concept:C1314792 | lld:lifeskim |
| pubmed-article:12359607 | lifeskim:mentions | umls-concept:C1413723 | lld:lifeskim |
| pubmed-article:12359607 | lifeskim:mentions | umls-concept:C0679622 | lld:lifeskim |
| pubmed-article:12359607 | lifeskim:mentions | umls-concept:C0205314 | lld:lifeskim |
| pubmed-article:12359607 | lifeskim:mentions | umls-concept:C2348519 | lld:lifeskim |
| pubmed-article:12359607 | pubmed:issue | 10 | lld:pubmed |
| pubmed-article:12359607 | pubmed:dateCreated | 2002-10-2 | lld:pubmed |
| pubmed-article:12359607 | pubmed:abstractText | To reexamine a large Albertan family previously reported with a progressive cone dystrophy with variable phenotype and to map the disorder using molecular genetic techniques. | lld:pubmed |
| pubmed-article:12359607 | pubmed:language | eng | lld:pubmed |
| pubmed-article:12359607 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:12359607 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:12359607 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:12359607 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:12359607 | pubmed:month | Oct | lld:pubmed |
| pubmed-article:12359607 | pubmed:issn | 0161-6420 | lld:pubmed |
| pubmed-article:12359607 | pubmed:author | pubmed-author:MacDonaldIan... | lld:pubmed |
| pubmed-article:12359607 | pubmed:author | pubmed-author:LinesMatthew... | lld:pubmed |
| pubmed-article:12359607 | pubmed:author | pubmed-author:HébertMarcM | lld:pubmed |
| pubmed-article:12359607 | pubmed:author | pubmed-author:McTaggartKerr... | lld:pubmed |
| pubmed-article:12359607 | pubmed:author | pubmed-author:FlynnSarah... | lld:pubmed |
| pubmed-article:12359607 | pubmed:author | pubmed-author:TennantMatthe... | lld:pubmed |
| pubmed-article:12359607 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:12359607 | pubmed:volume | 109 | lld:pubmed |
| pubmed-article:12359607 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:12359607 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:12359607 | pubmed:pagination | 1862-70 | lld:pubmed |
| pubmed-article:12359607 | pubmed:dateRevised | 2010-11-18 | lld:pubmed |
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| pubmed-article:12359607 | pubmed:meshHeading | pubmed-meshheading:12359607... | lld:pubmed |
| pubmed-article:12359607 | pubmed:year | 2002 | lld:pubmed |
| pubmed-article:12359607 | pubmed:articleTitle | Electrophysiologic and phenotypic features of an autosomal cone-rod dystrophy caused by a novel CRX mutation. | lld:pubmed |
| pubmed-article:12359607 | pubmed:affiliation | Department of Ophthalmology, University of Alberta Faculty of Medicine and Dentistry, Edmonton, AB, Canada. | lld:pubmed |
| pubmed-article:12359607 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:12359607 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| entrez-gene:1406 | entrezgene:pubmed | pubmed-article:12359607 | lld:entrezgene |
| http://linkedlifedata.com/r... | entrezgene:pubmed | pubmed-article:12359607 | lld:entrezgene |
| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:12359607 | lld:pubmed |
