Brittle cornea syndrome: recognition, molecular diagnosis and management.
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| Title: | Brittle cornea syndrome: recognition, molecular diagnosis and management. |
|---|---|
| Authors: | Burkitt Wright EM; Genetic Medicine, Institute of Human Development, Faculty of Medical and Human Sciences, University of Manchester, Manchester, UK. graeme.black@manchester.ac.uk., Porter LF, Spencer HL, Clayton-Smith J, Au L, Munier FL, Smithson S, Suri M, Rohrbach M, Manson FD, Black GC |
| Source: | Orphanet journal of rare diseases [Orphanet J Rare Dis] 2013 May 04; Vol. 8, pp. 68. Date of Electronic Publication: 2013 May 04. |
| Publication Type: | Journal Article; Research Support, Non-U.S. Gov't; Review |
| Journal Info: | Publisher: BioMed Central Country of Publication: England NLM ID: 101266602 Publication Model: Electronic Cited Medium: Internet ISSN: 1750-1172 (Electronic) Linking ISSN: 17501172 NLM ISO Abbreviation: Orphanet J Rare Dis Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
| FullText | Links: – Type: pdflink Text: Availability: 0 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 23642083 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Brittle cornea syndrome: recognition, molecular diagnosis and management. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Burkitt+Wright+EM%22">Burkitt Wright EM</searchLink>; Genetic Medicine, Institute of Human Development, Faculty of Medical and Human Sciences, University of Manchester, Manchester, UK. graeme.black@manchester.ac.uk.<br /><searchLink fieldCode="AU" term="%22Porter+LF%22">Porter LF</searchLink><br /><searchLink fieldCode="AU" term="%22Spencer+HL%22">Spencer HL</searchLink><br /><searchLink fieldCode="AU" term="%22Clayton-Smith+J%22">Clayton-Smith J</searchLink><br /><searchLink fieldCode="AU" term="%22Au+L%22">Au L</searchLink><br /><searchLink fieldCode="AU" term="%22Munier+FL%22">Munier FL</searchLink><br /><searchLink fieldCode="AU" term="%22Smithson+S%22">Smithson S</searchLink><br /><searchLink fieldCode="AU" term="%22Suri+M%22">Suri M</searchLink><br /><searchLink fieldCode="AU" term="%22Rohrbach+M%22">Rohrbach M</searchLink><br /><searchLink fieldCode="AU" term="%22Manson+FD%22">Manson FD</searchLink><br /><searchLink fieldCode="AU" term="%22Black+GC%22">Black GC</searchLink> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22101266602%22">Orphanet journal of rare diseases</searchLink> [Orphanet J Rare Dis] 2013 May 04; Vol. 8, pp. 68. <i>Date of Electronic Publication: </i>2013 May 04. – Name: TypePub Label: Publication Type Group: TypPub Data: Journal Article; Research Support, Non-U.S. Gov't; Review – Name: TitleSource Label: Journal Info Group: Src Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22BioMed+Central%22">BioMed Central </searchLink><i>Country of Publication: </i>England <i>NLM ID: </i>101266602 <i>Publication Model: </i>Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1750-1172 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2217501172%22">17501172 </searchLink><i>NLM ISO Abbreviation: </i>Orphanet J Rare Dis <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=23642083 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1186/1750-1172-8-68 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 68 Titles: – TitleFull: Brittle cornea syndrome: recognition, molecular diagnosis and management. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Burkitt Wright EM – PersonEntity: Name: NameFull: Porter LF – PersonEntity: Name: NameFull: Spencer HL – PersonEntity: Name: NameFull: Clayton-Smith J – PersonEntity: Name: NameFull: Au L – PersonEntity: Name: NameFull: Munier FL – PersonEntity: Name: NameFull: Smithson S – PersonEntity: Name: NameFull: Suri M – PersonEntity: Name: NameFull: Rohrbach M – PersonEntity: Name: NameFull: Manson FD – PersonEntity: Name: NameFull: Black GC IsPartOfRelationships: – BibEntity: Dates: – D: 04 M: 05 Text: 2013 May 04 Type: published Y: 2013 Identifiers: – Type: issn-electronic Value: 1750-1172 Numbering: – Type: volume Value: 8 Titles: – TitleFull: Orphanet journal of rare diseases Type: main |
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