| pubmed-article:16785853 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:16785853 | lifeskim:mentions | umls-concept:C0030705 | lld:lifeskim |
| pubmed-article:16785853 | lifeskim:mentions | umls-concept:C0152035 | lld:lifeskim |
| pubmed-article:16785853 | lifeskim:mentions | umls-concept:C1418276 | lld:lifeskim |
| pubmed-article:16785853 | lifeskim:mentions | umls-concept:C0003076 | lld:lifeskim |
| pubmed-article:16785853 | lifeskim:mentions | umls-concept:C0026882 | lld:lifeskim |
| pubmed-article:16785853 | lifeskim:mentions | umls-concept:C0205396 | lld:lifeskim |
| pubmed-article:16785853 | lifeskim:mentions | umls-concept:C0679622 | lld:lifeskim |
| pubmed-article:16785853 | lifeskim:mentions | umls-concept:C0205314 | lld:lifeskim |
| pubmed-article:16785853 | pubmed:dateCreated | 2006-6-20 | lld:pubmed |
| pubmed-article:16785853 | pubmed:abstractText | Mutations in PAX6 are the major cause of aniridia. Only a few PAX6 mutations in Chinese have been reported. This study is to identify novel mutations in PAX6 of Chinese patients with aniridia. | lld:pubmed |
| pubmed-article:16785853 | pubmed:language | eng | lld:pubmed |
| pubmed-article:16785853 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:16785853 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:16785853 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:16785853 | pubmed:issn | 1090-0535 | lld:pubmed |
| pubmed-article:16785853 | pubmed:author | pubmed-author:ZhangQingjion... | lld:pubmed |
| pubmed-article:16785853 | pubmed:author | pubmed-author:XiaoXueshanX | lld:pubmed |
| pubmed-article:16785853 | pubmed:author | pubmed-author:GuoXiangmingX | lld:pubmed |
| pubmed-article:16785853 | pubmed:author | pubmed-author:JiaXiaoyunX | lld:pubmed |
| pubmed-article:16785853 | pubmed:author | pubmed-author:LiShiqiangS | lld:pubmed |
| pubmed-article:16785853 | pubmed:author | pubmed-author:WangPanfengP | lld:pubmed |
| pubmed-article:16785853 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:16785853 | pubmed:volume | 12 | lld:pubmed |
| pubmed-article:16785853 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:16785853 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:16785853 | pubmed:pagination | 644-8 | lld:pubmed |
| pubmed-article:16785853 | pubmed:dateRevised | 2006-11-15 | lld:pubmed |
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| pubmed-article:16785853 | pubmed:meshHeading | pubmed-meshheading:16785853... | lld:pubmed |
| pubmed-article:16785853 | pubmed:meshHeading | pubmed-meshheading:16785853... | lld:pubmed |
| pubmed-article:16785853 | pubmed:meshHeading | pubmed-meshheading:16785853... | lld:pubmed |
| pubmed-article:16785853 | pubmed:meshHeading | pubmed-meshheading:16785853... | lld:pubmed |
| pubmed-article:16785853 | pubmed:year | 2006 | lld:pubmed |
| pubmed-article:16785853 | pubmed:articleTitle | Novel mutations of the PAX6 gene identified in Chinese patients with aniridia. | lld:pubmed |
| pubmed-article:16785853 | pubmed:affiliation | Key Laboratory of Ophthalmology of the Ministry of Education and Zhongshan Ophthalmic Center, Sun Yat-sen University, Guangzhou, People's Republic of China. | lld:pubmed |
| pubmed-article:16785853 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:16785853 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:16785853 | lld:pubmed |
