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pubmed-article:12928282 | lifeskim:mentions | umls-concept:C0337810 | lld:lifeskim |
pubmed-article:12928282 | lifeskim:mentions | umls-concept:C0017337 | lld:lifeskim |
pubmed-article:12928282 | lifeskim:mentions | umls-concept:C0026882 | lld:lifeskim |
pubmed-article:12928282 | lifeskim:mentions | umls-concept:C1419764 | lld:lifeskim |
pubmed-article:12928282 | lifeskim:mentions | umls-concept:C0332281 | lld:lifeskim |
pubmed-article:12928282 | lifeskim:mentions | umls-concept:C0271091 | lld:lifeskim |
pubmed-article:12928282 | lifeskim:mentions | umls-concept:C0205210 | lld:lifeskim |
pubmed-article:12928282 | lifeskim:mentions | umls-concept:C2348519 | lld:lifeskim |
pubmed-article:12928282 | pubmed:issue | 9 | lld:pubmed |
pubmed-article:12928282 | pubmed:dateCreated | 2003-8-20 | lld:pubmed |
pubmed-article:12928282 | pubmed:abstractText | To describe the clinical phenotype of X linked juvenile retinoschisis in eight Italian families with six different mutations in the XLRS1 gene. | lld:pubmed |
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pubmed-article:12928282 | pubmed:language | eng | lld:pubmed |
pubmed-article:12928282 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:12928282 | pubmed:citationSubset | IM | lld:pubmed |
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pubmed-article:12928282 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:12928282 | pubmed:month | Sep | lld:pubmed |
pubmed-article:12928282 | pubmed:issn | 0007-1161 | lld:pubmed |
pubmed-article:12928282 | pubmed:author | pubmed-author:BrancatoRR | lld:pubmed |
pubmed-article:12928282 | pubmed:author | pubmed-author:CennamoGG | lld:pubmed |
pubmed-article:12928282 | pubmed:author | pubmed-author:RinaldiEE | lld:pubmed |
pubmed-article:12928282 | pubmed:author | pubmed-author:de CrecchioGG | lld:pubmed |
pubmed-article:12928282 | pubmed:author | pubmed-author:BanfiSS | lld:pubmed |
pubmed-article:12928282 | pubmed:author | pubmed-author:NestiAA | lld:pubmed |
pubmed-article:12928282 | pubmed:author | pubmed-author:SimonelliFF | lld:pubmed |
pubmed-article:12928282 | pubmed:author | pubmed-author:ManittoM PMP | lld:pubmed |
pubmed-article:12928282 | pubmed:author | pubmed-author:CiccodicolaAA | lld:pubmed |
pubmed-article:12928282 | pubmed:author | pubmed-author:TestaFF | lld:pubmed |
pubmed-article:12928282 | pubmed:author | pubmed-author:ZivielloCC | lld:pubmed |
pubmed-article:12928282 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:12928282 | pubmed:volume | 87 | lld:pubmed |
pubmed-article:12928282 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:12928282 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:12928282 | pubmed:pagination | 1130-4 | lld:pubmed |
pubmed-article:12928282 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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pubmed-article:12928282 | pubmed:year | 2003 | lld:pubmed |
pubmed-article:12928282 | pubmed:articleTitle | Clinical features of X linked juvenile retinoschisis associated with new mutations in the XLRS1 gene in Italian families. | lld:pubmed |
pubmed-article:12928282 | pubmed:affiliation | Department of Ophthalmology, Seconda Università di Napoli, Naples, Italy. Telethon Institute of Genetics and Medicine (TIGEM), Italy. franctes@tin.it | lld:pubmed |
pubmed-article:12928282 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:12928282 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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