Brittle cornea syndrome: recognition, molecular diagnosis and management.
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| Title: | Brittle cornea syndrome: recognition, molecular diagnosis and management. |
|---|---|
| Authors: | Burkitt Wright, Emma M. M.1,2, Porter, Louise F.1,2, Spencer, Helen L.3, Clayton-Smith, Jill1,2, Au, Leon4, Munier, Francis L.5, Smithson, Sarah6, Suri, Mohnish7, Rohrbach, Marianne8, Manson, Forbes D. C.1, Black, Graeme C. M.1,2 graeme.black@manchester.ac.uk |
| Source: | Orphanet Journal of Rare Diseases. 2013, Vol. 8 Issue 1, p1-11. 11p. 1 Color Photograph, 2 Diagrams, 2 Charts, 1 Graph. |
| Database: | Academic Search Ultimate |
| FullText | Links: – Type: pdflink Text: Availability: 0 |
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| Header | DbId: asn DbLabel: Academic Search Ultimate An: 88013852 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=88013852 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1186/1750-1172-8-68 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 11 StartPage: 1 Titles: – TitleFull: Brittle cornea syndrome: recognition, molecular diagnosis and management. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Burkitt Wright, Emma M. M. – PersonEntity: Name: NameFull: Porter, Louise F. – PersonEntity: Name: NameFull: Spencer, Helen L. – PersonEntity: Name: NameFull: Clayton-Smith, Jill – PersonEntity: Name: NameFull: Au, Leon – PersonEntity: Name: NameFull: Munier, Francis L. – PersonEntity: Name: NameFull: Smithson, Sarah – PersonEntity: Name: NameFull: Suri, Mohnish – PersonEntity: Name: NameFull: Rohrbach, Marianne – PersonEntity: Name: NameFull: Manson, Forbes D. C. – PersonEntity: Name: NameFull: Black, Graeme C. M. IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 06 Text: 2013 Type: published Y: 2013 Identifiers: – Type: issn-print Value: 17501172 Numbering: – Type: volume Value: 8 – Type: issue Value: 1 Titles: – TitleFull: Orphanet Journal of Rare Diseases Type: main |
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