| pubmed-article:14566650 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:14566650 | lifeskim:mentions | umls-concept:C0015576 | lld:lifeskim |
| pubmed-article:14566650 | lifeskim:mentions | umls-concept:C0008525 | lld:lifeskim |
| pubmed-article:14566650 | lifeskim:mentions | umls-concept:C0017337 | lld:lifeskim |
| pubmed-article:14566650 | lifeskim:mentions | umls-concept:C1413394 | lld:lifeskim |
| pubmed-article:14566650 | lifeskim:mentions | umls-concept:C1853719 | lld:lifeskim |
| pubmed-article:14566650 | lifeskim:mentions | umls-concept:C0079380 | lld:lifeskim |
| pubmed-article:14566650 | lifeskim:mentions | umls-concept:C1742737 | lld:lifeskim |
| pubmed-article:14566650 | pubmed:issue | 4 | lld:pubmed |
| pubmed-article:14566650 | pubmed:dateCreated | 2003-10-20 | lld:pubmed |
| pubmed-article:14566650 | pubmed:abstractText | To perform genotype-phenotype correlations in a family with choroideremia. | lld:pubmed |
| pubmed-article:14566650 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:14566650 | pubmed:language | eng | lld:pubmed |
| pubmed-article:14566650 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:14566650 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:14566650 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:14566650 | pubmed:month | Dec | lld:pubmed |
| pubmed-article:14566650 | pubmed:issn | 1381-6810 | lld:pubmed |
| pubmed-article:14566650 | pubmed:author | pubmed-author:RudolphGünthe... | lld:pubmed |
| pubmed-article:14566650 | pubmed:author | pubmed-author:LorenzBirgitB | lld:pubmed |
| pubmed-article:14566650 | pubmed:author | pubmed-author:LangGabriele... | lld:pubmed |
| pubmed-article:14566650 | pubmed:author | pubmed-author:HaritoglouChr... | lld:pubmed |
| pubmed-article:14566650 | pubmed:author | pubmed-author:PreisingMarku... | lld:pubmed |
| pubmed-article:14566650 | pubmed:author | pubmed-author:KalpadakisPet... | lld:pubmed |
| pubmed-article:14566650 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:14566650 | pubmed:volume | 24 | lld:pubmed |
| pubmed-article:14566650 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:14566650 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:14566650 | pubmed:pagination | 203-14 | lld:pubmed |
| pubmed-article:14566650 | pubmed:dateRevised | 2008-11-21 | lld:pubmed |
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| pubmed-article:14566650 | pubmed:meshHeading | pubmed-meshheading:14566650... | lld:pubmed |
| pubmed-article:14566650 | pubmed:year | 2003 | lld:pubmed |
| pubmed-article:14566650 | pubmed:articleTitle | Phenotypic variability in three carriers from a family with choroideremia and a frameshift mutation 1388delCCinsG in the REP-1 gene. | lld:pubmed |
| pubmed-article:14566650 | pubmed:affiliation | Kooperationsgruppe Ophthalmogenetik der LMU und GSF University Eye Hospital, LMU, München, Germany. Guenther.Rudolph@ak-i.med.uni-muenchen.de | lld:pubmed |
| pubmed-article:14566650 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:14566650 | pubmed:publicationType | Case Reports | lld:pubmed |
| pubmed-article:14566650 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| entrez-gene:1121 | entrezgene:pubmed | pubmed-article:14566650 | lld:entrezgene |
| http://linkedlifedata.com/r... | entrezgene:pubmed | pubmed-article:14566650 | lld:entrezgene |
| lhgdn:association:62324 | lhgdn:found_in | pubmed-article:14566650 | lld:lhgdn |
| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:14566650 | lld:pubmed |
