pubmed-article:18587493 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:18587493 | lifeskim:mentions | umls-concept:C0422792 | lld:lifeskim |
pubmed-article:18587493 | lifeskim:mentions | umls-concept:C0015576 | lld:lifeskim |
pubmed-article:18587493 | lifeskim:mentions | umls-concept:C0086543 | lld:lifeskim |
pubmed-article:18587493 | lifeskim:mentions | umls-concept:C0026882 | lld:lifeskim |
pubmed-article:18587493 | lifeskim:mentions | umls-concept:C0332281 | lld:lifeskim |
pubmed-article:18587493 | lifeskim:mentions | umls-concept:C1415075 | lld:lifeskim |
pubmed-article:18587493 | lifeskim:mentions | umls-concept:C0029053 | lld:lifeskim |
pubmed-article:18587493 | lifeskim:mentions | umls-concept:C0439659 | lld:lifeskim |
pubmed-article:18587493 | pubmed:dateCreated | 2008-6-30 | lld:pubmed |
pubmed-article:18587493 | pubmed:abstractText | To detect the underlying genetic defect in a family with three members in two generations affected with bilateral congenital cataract. | lld:pubmed |
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pubmed-article:18587493 | pubmed:language | eng | lld:pubmed |
pubmed-article:18587493 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18587493 | pubmed:citationSubset | IM | lld:pubmed |
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pubmed-article:18587493 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:18587493 | pubmed:issn | 1090-0535 | lld:pubmed |
pubmed-article:18587493 | pubmed:author | pubmed-author:XXX | lld:pubmed |
pubmed-article:18587493 | pubmed:author | pubmed-author:SinghDaljitD | lld:pubmed |
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pubmed-article:18587493 | pubmed:author | pubmed-author:SperlingKarlK | lld:pubmed |
pubmed-article:18587493 | pubmed:author | pubmed-author:SinghJai... | lld:pubmed |
pubmed-article:18587493 | pubmed:issnType | Electronic | lld:pubmed |
pubmed-article:18587493 | pubmed:volume | 14 | lld:pubmed |
pubmed-article:18587493 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:18587493 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:18587493 | pubmed:pagination | 1171-5 | lld:pubmed |
pubmed-article:18587493 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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pubmed-article:18587493 | pubmed:year | 2008 | lld:pubmed |
pubmed-article:18587493 | pubmed:articleTitle | A mutation in GJA8 (p.P88Q) is associated with "balloon-like" cataract with Y-sutural opacities in a family of Indian origin. | lld:pubmed |
pubmed-article:18587493 | pubmed:affiliation | Centre for Genetic Disorders, Guru Nanak Dev University, Amritsar, India. vanita_kumar@yahoo.com | lld:pubmed |
pubmed-article:18587493 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:18587493 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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