| pubmed-article:21600657 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:21600657 | lifeskim:mentions | umls-concept:C0000768 | lld:lifeskim |
| pubmed-article:21600657 | lifeskim:mentions | umls-concept:C0020302 | lld:lifeskim |
| pubmed-article:21600657 | lifeskim:mentions | umls-concept:C0041582 | lld:lifeskim |
| pubmed-article:21600657 | lifeskim:mentions | umls-concept:C0026882 | lld:lifeskim |
| pubmed-article:21600657 | lifeskim:mentions | umls-concept:C0348014 | lld:lifeskim |
| pubmed-article:21600657 | lifeskim:mentions | umls-concept:C0679622 | lld:lifeskim |
| pubmed-article:21600657 | lifeskim:mentions | umls-concept:C0205314 | lld:lifeskim |
| pubmed-article:21600657 | pubmed:issue | 9 | lld:pubmed |
| pubmed-article:21600657 | pubmed:dateCreated | 2011-9-5 | lld:pubmed |
| pubmed-article:21600657 | pubmed:abstractText | To determine the prevalence of CYP1B1 mutations in a cohort of patients with congenital corneal opacification (CCO), infantile glaucoma, or both and to describe a developmental CCO associated with CYP1B1 mutation that may explain von Hippel's original description of an internal ulcer. | lld:pubmed |
| pubmed-article:21600657 | pubmed:language | eng | lld:pubmed |
| pubmed-article:21600657 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21600657 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:21600657 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21600657 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21600657 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:21600657 | pubmed:month | Sep | lld:pubmed |
| pubmed-article:21600657 | pubmed:issn | 1549-4713 | lld:pubmed |
| pubmed-article:21600657 | pubmed:author | pubmed-author:KhawPeng TPT | lld:pubmed |
| pubmed-article:21600657 | pubmed:author | pubmed-author:NischalKen... | lld:pubmed |
| pubmed-article:21600657 | pubmed:author | pubmed-author:Russell-Eggit... | lld:pubmed |
| pubmed-article:21600657 | pubmed:author | pubmed-author:SowdenJane... | lld:pubmed |
| pubmed-article:21600657 | pubmed:author | pubmed-author:Bitner-Glindz... | lld:pubmed |
| pubmed-article:21600657 | pubmed:author | pubmed-author:JacquesThomas... | lld:pubmed |
| pubmed-article:21600657 | pubmed:author | pubmed-author:KelbermanDani... | lld:pubmed |
| pubmed-article:21600657 | pubmed:author | pubmed-author:IslamLilyL | lld:pubmed |
| pubmed-article:21600657 | pubmed:copyrightInfo | Copyright © 2011 American Academy of Ophthalmology. Published by Elsevier Inc. All rights reserved. | lld:pubmed |
| pubmed-article:21600657 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:21600657 | pubmed:volume | 118 | lld:pubmed |
| pubmed-article:21600657 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:21600657 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:21600657 | pubmed:pagination | 1865-73 | lld:pubmed |
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| pubmed-article:21600657 | pubmed:meshHeading | pubmed-meshheading:21600657... | lld:pubmed |
| pubmed-article:21600657 | pubmed:year | 2011 | lld:pubmed |
| pubmed-article:21600657 | pubmed:articleTitle | CYP1B1-related anterior segment developmental anomalies novel mutations for infantile glaucoma and von Hippel's ulcer revisited. | lld:pubmed |
| pubmed-article:21600657 | pubmed:affiliation | Ulverscroft Vision Research Group, University College London Institute of Child Health, London, and Great Ormond Street Hospital for Children NHS Trust, London, United Kingdom. | lld:pubmed |
| pubmed-article:21600657 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:21600657 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| entrez-gene:1545 | entrezgene:pubmed | pubmed-article:21600657 | lld:entrezgene |
| http://linkedlifedata.com/r... | entrezgene:pubmed | pubmed-article:21600657 | lld:entrezgene |
