| pubmed-article:16186331 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:16186331 | lifeskim:mentions | umls-concept:C2350017 | lld:lifeskim |
| pubmed-article:16186331 | lifeskim:mentions | umls-concept:C0035334 | lld:lifeskim |
| pubmed-article:16186331 | lifeskim:mentions | umls-concept:C0854723 | lld:lifeskim |
| pubmed-article:16186331 | lifeskim:mentions | umls-concept:C0017258 | lld:lifeskim |
| pubmed-article:16186331 | lifeskim:mentions | umls-concept:C1708726 | lld:lifeskim |
| pubmed-article:16186331 | lifeskim:mentions | umls-concept:C0443147 | lld:lifeskim |
| pubmed-article:16186331 | lifeskim:mentions | umls-concept:C0024779 | lld:lifeskim |
| pubmed-article:16186331 | lifeskim:mentions | umls-concept:C0679622 | lld:lifeskim |
| pubmed-article:16186331 | lifeskim:mentions | umls-concept:C1704638 | lld:lifeskim |
| pubmed-article:16186331 | lifeskim:mentions | umls-concept:C0205314 | lld:lifeskim |
| pubmed-article:16186331 | lifeskim:mentions | umls-concept:C0330095 | lld:lifeskim |
| pubmed-article:16186331 | pubmed:issue | 10 | lld:pubmed |
| pubmed-article:16186331 | pubmed:dateCreated | 2005-9-27 | lld:pubmed |
| pubmed-article:16186331 | pubmed:abstractText | To characterize clinically and genetically a four-generation Italian family with autosomal dominant retinal dystrophy. | lld:pubmed |
| pubmed-article:16186331 | pubmed:language | eng | lld:pubmed |
| pubmed-article:16186331 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:16186331 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:16186331 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:16186331 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:16186331 | pubmed:month | Oct | lld:pubmed |
| pubmed-article:16186331 | pubmed:issn | 0146-0404 | lld:pubmed |
| pubmed-article:16186331 | pubmed:author | pubmed-author:ValenteEnza... | lld:pubmed |
| pubmed-article:16186331 | pubmed:author | pubmed-author:BrancatiFranc... | lld:pubmed |
| pubmed-article:16186331 | pubmed:author | pubmed-author:CaputoViviana... | lld:pubmed |
| pubmed-article:16186331 | pubmed:author | pubmed-author:DallapiccolaB... | lld:pubmed |
| pubmed-article:16186331 | pubmed:author | pubmed-author:ClementiMauri... | lld:pubmed |
| pubmed-article:16186331 | pubmed:author | pubmed-author:TormeneAlma... | lld:pubmed |
| pubmed-article:16186331 | pubmed:author | pubmed-author:CastoriMarcoM | lld:pubmed |
| pubmed-article:16186331 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:16186331 | pubmed:volume | 46 | lld:pubmed |
| pubmed-article:16186331 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:16186331 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:16186331 | pubmed:pagination | 3539-44 | lld:pubmed |
| pubmed-article:16186331 | pubmed:dateRevised | 2010-11-18 | lld:pubmed |
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| pubmed-article:16186331 | pubmed:meshHeading | pubmed-meshheading:16186331... | lld:pubmed |
| pubmed-article:16186331 | pubmed:meshHeading | pubmed-meshheading:16186331... | lld:pubmed |
| pubmed-article:16186331 | pubmed:meshHeading | pubmed-meshheading:16186331... | lld:pubmed |
| pubmed-article:16186331 | pubmed:meshHeading | pubmed-meshheading:16186331... | lld:pubmed |
| pubmed-article:16186331 | pubmed:meshHeading | pubmed-meshheading:16186331... | lld:pubmed |
| pubmed-article:16186331 | pubmed:meshHeading | pubmed-meshheading:16186331... | lld:pubmed |
| pubmed-article:16186331 | pubmed:meshHeading | pubmed-meshheading:16186331... | lld:pubmed |
| pubmed-article:16186331 | pubmed:meshHeading | pubmed-meshheading:16186331... | lld:pubmed |
| pubmed-article:16186331 | pubmed:meshHeading | pubmed-meshheading:16186331... | lld:pubmed |
| pubmed-article:16186331 | pubmed:meshHeading | pubmed-meshheading:16186331... | lld:pubmed |
| pubmed-article:16186331 | pubmed:meshHeading | pubmed-meshheading:16186331... | lld:pubmed |
| pubmed-article:16186331 | pubmed:year | 2005 | lld:pubmed |
| pubmed-article:16186331 | pubmed:articleTitle | A novel locus for autosomal dominant cone and cone-rod dystrophies maps to the 6p gene cluster of retinal dystrophies. | lld:pubmed |
| pubmed-article:16186331 | pubmed:affiliation | Istituto di Ricovero e Cura a Carattere Scientifico Casa Sollievo della Sofferenza (IRCCS CSS), Mendel Institute, Rome, Italy. | lld:pubmed |
| pubmed-article:16186331 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:16186331 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
