| Molecular genetic approaches to the analysis of human ophthalmic disease. | |
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MedLine Citation:
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PMID: 3331606 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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In this review of the recent literature, the contribution that the new techniques of molecular genetics has made in the analysis and diagnosis of human ophthalmic conditions is presented and discussed. Among the disorders reviewed are X-linked retinitis pigmentosa, Norrie's disease, gyrate atrophy and retinoblastoma, and there are also sections on crystallins and visual pigments. |
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Authors:
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D N Cooper; M Jay; S Bhattacharya; B Jay |
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Publication Detail:
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Type: Journal Article; Review |
Journal Detail:
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Title: Eye (London, England) Volume: 1 ( Pt 6) ISSN: 0950-222X ISO Abbreviation: Eye (Lond) Publication Date: 1987 |
Date Detail:
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Created Date: 1988-10-13 Completed Date: 1988-10-13 Revised Date: 2009-11-03 |
Medline Journal Info:
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Nlm Unique ID: 8703986 Medline TA: Eye (Lond) Country: ENGLAND |
Other Details:
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Languages: eng Pagination: 699-721 Citation Subset: IM |
Affiliation:
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Haematology Department, King's College Hospital School of Medicine, Denmark Hill, London. |
Export Citation:
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APA/MLA Format Download EndNote Download BibTex |
| MeSH Terms | |
Descriptor/Qualifier:
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Chromosome Mapping Crystallins / genetics DNA, Recombinant Eye Diseases / genetics* Eye Neoplasms / genetics Female Humans Male Molecular Biology Retinal Pigments / genetics Retinitis Pigmentosa / genetics Retinoblastoma / genetics Vision, Ocular |
| Chemical | |
Reg. No./Substance:
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0/Crystallins; 0/DNA, Recombinant; 0/Retinal Pigments |
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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