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| pubmed-article:11139690 | lifeskim:mentions | umls-concept:C1720675 | lld:lifeskim |
| pubmed-article:11139690 | pubmed:issue | 10 | lld:pubmed |
| pubmed-article:11139690 | pubmed:dateCreated | 2001-2-20 | lld:pubmed |
| pubmed-article:11139690 | pubmed:abstractText | To evaluate the occurrence and inheritance of various types of pigmentary retinopathy in patients followed at the outpatient clinic in the university hospital, Montpellier, France. To characterize genes and mutations causing these conditions. | lld:pubmed |
| pubmed-article:11139690 | pubmed:language | fre | lld:pubmed |
| pubmed-article:11139690 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:11139690 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:11139690 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:11139690 | pubmed:month | Dec | lld:pubmed |
| pubmed-article:11139690 | pubmed:issn | 0181-5512 | lld:pubmed |
| pubmed-article:11139690 | pubmed:author | pubmed-author:ArnaudBB | lld:pubmed |
| pubmed-article:11139690 | pubmed:author | pubmed-author:ClaustresMM | lld:pubmed |
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| pubmed-article:11139690 | pubmed:author | pubmed-author:TufferySS | lld:pubmed |
| pubmed-article:11139690 | pubmed:author | pubmed-author:HamelC PCP | lld:pubmed |
| pubmed-article:11139690 | pubmed:author | pubmed-author:MarlhensFF | lld:pubmed |
| pubmed-article:11139690 | pubmed:author | pubmed-author:BazalgetteCC | lld:pubmed |
| pubmed-article:11139690 | pubmed:author | pubmed-author:Schmitt-Berna... | lld:pubmed |
| pubmed-article:11139690 | pubmed:author | pubmed-author:BareilCC | lld:pubmed |
| pubmed-article:11139690 | pubmed:author | pubmed-author:BeaufrèreLL | lld:pubmed |
| pubmed-article:11139690 | pubmed:author | pubmed-author:GriffoinJ MJM | lld:pubmed |
| pubmed-article:11139690 | pubmed:author | pubmed-author:EliaouCC | lld:pubmed |
| pubmed-article:11139690 | pubmed:author | pubmed-author:LasquellecLL | lld:pubmed |
| pubmed-article:11139690 | pubmed:author | pubmed-author:DuvalP APA | lld:pubmed |
| pubmed-article:11139690 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:11139690 | pubmed:volume | 23 | lld:pubmed |
| pubmed-article:11139690 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:11139690 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:11139690 | pubmed:pagination | 985-95 | lld:pubmed |
| pubmed-article:11139690 | pubmed:dateRevised | 2006-11-20 | lld:pubmed |
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| pubmed-article:11139690 | pubmed:year | 2000 | lld:pubmed |
| pubmed-article:11139690 | pubmed:articleTitle | [Molecular genetics of pigmentary retinopathies: identification of mutations in CHM, RDS, RHO, RPE65, USH2A and XLRS1 genes]. | lld:pubmed |
| pubmed-article:11139690 | pubmed:affiliation | Laboratoire de Neurobiologie, Inserm U. 254, 71, rue de Navacelles, 34090 Montpellier. hamel@montp.inserm.fr | lld:pubmed |
| pubmed-article:11139690 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:11139690 | pubmed:publicationType | English Abstract | lld:pubmed |
| pubmed-article:11139690 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| pubmed-article:11139690 | pubmed:publicationType | Multicenter Study | lld:pubmed |
| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:11139690 | lld:pubmed |
