| pubmed-article:9152134 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:9152134 | lifeskim:mentions | umls-concept:C0020792 | lld:lifeskim |
| pubmed-article:9152134 | lifeskim:mentions | umls-concept:C0035344 | lld:lifeskim |
| pubmed-article:9152134 | lifeskim:mentions | umls-concept:C0017337 | lld:lifeskim |
| pubmed-article:9152134 | lifeskim:mentions | umls-concept:C0266526 | lld:lifeskim |
| pubmed-article:9152134 | lifeskim:mentions | umls-concept:C0332281 | lld:lifeskim |
| pubmed-article:9152134 | lifeskim:mentions | umls-concept:C0599155 | lld:lifeskim |
| pubmed-article:9152134 | lifeskim:mentions | umls-concept:C0205179 | lld:lifeskim |
| pubmed-article:9152134 | pubmed:issue | 5 | lld:pubmed |
| pubmed-article:9152134 | pubmed:dateCreated | 1997-5-23 | lld:pubmed |
| pubmed-article:9152134 | pubmed:abstractText | Retinopathy of prematurity (ROP) is a retinal vascular disease occurring in infants with short gestational age and low birth weight and can lead to retinal detachment (ROP stages 4 and 5). X-linked familial exudative vitreoretinopathy is phenotypically similar to ROP and has been associated with mutations in the Norrie disease (ND) gene in some cases. | lld:pubmed |
| pubmed-article:9152134 | pubmed:language | eng | lld:pubmed |
| pubmed-article:9152134 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9152134 | pubmed:citationSubset | AIM | lld:pubmed |
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| pubmed-article:9152134 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:9152134 | pubmed:month | May | lld:pubmed |
| pubmed-article:9152134 | pubmed:issn | 0003-9950 | lld:pubmed |
| pubmed-article:9152134 | pubmed:author | pubmed-author:LimPP | lld:pubmed |
| pubmed-article:9152134 | pubmed:author | pubmed-author:TreseM TMT | lld:pubmed |
| pubmed-article:9152134 | pubmed:author | pubmed-author:HartzerM KMK | lld:pubmed |
| pubmed-article:9152134 | pubmed:author | pubmed-author:ShastryB SBS | lld:pubmed |
| pubmed-article:9152134 | pubmed:author | pubmed-author:PendergastS... | lld:pubmed |
| pubmed-article:9152134 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:9152134 | pubmed:volume | 115 | lld:pubmed |
| pubmed-article:9152134 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:9152134 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:9152134 | pubmed:pagination | 651-5 | lld:pubmed |
| pubmed-article:9152134 | pubmed:dateRevised | 2011-11-17 | lld:pubmed |
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| pubmed-article:9152134 | pubmed:meshHeading | pubmed-meshheading:9152134-... | lld:pubmed |
| pubmed-article:9152134 | pubmed:year | 1997 | lld:pubmed |
| pubmed-article:9152134 | pubmed:articleTitle | Identification of missense mutations in the Norrie disease gene associated with advanced retinopathy of prematurity. | lld:pubmed |
| pubmed-article:9152134 | pubmed:affiliation | Eye Research Institute, Oakland University, Rochester, Mich, USA. | lld:pubmed |
| pubmed-article:9152134 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:9152134 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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