Hereditary vascular retinopathy, cerebroretinal vasculopathy, and hereditary endotheliopathy with retinopathy, nephropathy, and stroke map to a single locus on chromosome 3p21.1-p21.3.
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| Title: | Hereditary vascular retinopathy, cerebroretinal vasculopathy, and hereditary endotheliopathy with retinopathy, nephropathy, and stroke map to a single locus on chromosome 3p21.1-p21.3. |
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| Authors: | Ophoff RA; Departments of Human and Clinical Genetics and Neurology, Leiden University Medical Center, Leiden, The Netherlands., DeYoung J, Service SK, Joosse M, Caffo NA, Sandkuijl LA, Terwindt GM, Haan J, van den Maagdenberg AM, Jen J, Baloh RW, Barilla-LaBarca ML, Saccone NL, Atkinson JP, Ferrari MD, Freimer NB, Frants RR |
| Source: | American journal of human genetics [Am J Hum Genet] 2001 Aug; Vol. 69 (2), pp. 447-53. Date of Electronic Publication: 2001 Jun 28. |
| Publication Type: | Journal Article; Research Support, U.S. Gov't, P.H.S. |
| Journal Info: | Publisher: Cell Press Country of Publication: United States NLM ID: 0370475 Publication Model: Print-Electronic Cited Medium: Print ISSN: 0002-9297 (Print) Linking ISSN: 00029297 NLM ISO Abbreviation: Am J Hum Genet Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
| FullText | Text: Availability: 0 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 11438888 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Hereditary vascular retinopathy, cerebroretinal vasculopathy, and hereditary endotheliopathy with retinopathy, nephropathy, and stroke map to a single locus on chromosome 3p21.1-p21.3. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Ophoff+RA%22">Ophoff RA</searchLink>; Departments of Human and Clinical Genetics and Neurology, Leiden University Medical Center, Leiden, The Netherlands.<br /><searchLink fieldCode="AU" term="%22DeYoung+J%22">DeYoung J</searchLink><br /><searchLink fieldCode="AU" term="%22Service+SK%22">Service SK</searchLink><br /><searchLink fieldCode="AU" term="%22Joosse+M%22">Joosse M</searchLink><br /><searchLink fieldCode="AU" term="%22Caffo+NA%22">Caffo NA</searchLink><br /><searchLink fieldCode="AU" term="%22Sandkuijl+LA%22">Sandkuijl LA</searchLink><br /><searchLink fieldCode="AU" term="%22Terwindt+GM%22">Terwindt GM</searchLink><br /><searchLink fieldCode="AU" term="%22Haan+J%22">Haan J</searchLink><br /><searchLink fieldCode="AU" term="%22van+den+Maagdenberg+AM%22">van den Maagdenberg AM</searchLink><br /><searchLink fieldCode="AU" term="%22Jen+J%22">Jen J</searchLink><br /><searchLink fieldCode="AU" term="%22Baloh+RW%22">Baloh RW</searchLink><br /><searchLink fieldCode="AU" term="%22Barilla-LaBarca+ML%22">Barilla-LaBarca ML</searchLink><br /><searchLink fieldCode="AU" term="%22Saccone+NL%22">Saccone NL</searchLink><br /><searchLink fieldCode="AU" term="%22Atkinson+JP%22">Atkinson JP</searchLink><br /><searchLink fieldCode="AU" term="%22Ferrari+MD%22">Ferrari MD</searchLink><br /><searchLink fieldCode="AU" term="%22Freimer+NB%22">Freimer NB</searchLink><br /><searchLink fieldCode="AU" term="%22Frants+RR%22">Frants RR</searchLink> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%220370475%22">American journal of human genetics</searchLink> [Am J Hum Genet] 2001 Aug; Vol. 69 (2), pp. 447-53. <i>Date of Electronic Publication: </i>2001 Jun 28. – Name: TypePub Label: Publication Type Group: TypPub Data: Journal Article; Research Support, U.S. Gov't, P.H.S. – Name: TitleSource Label: Journal Info Group: Src Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Cell+Press%22">Cell Press </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>0370475 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Print <i>ISSN: </i>0002-9297 (Print) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2200029297%22">00029297 </searchLink><i>NLM ISO Abbreviation: </i>Am J Hum Genet <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=11438888 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1086/321975 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 447 Titles: – TitleFull: Hereditary vascular retinopathy, cerebroretinal vasculopathy, and hereditary endotheliopathy with retinopathy, nephropathy, and stroke map to a single locus on chromosome 3p21.1-p21.3. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Ophoff RA – PersonEntity: Name: NameFull: DeYoung J – PersonEntity: Name: NameFull: Service SK – PersonEntity: Name: NameFull: Joosse M – PersonEntity: Name: NameFull: Caffo NA – PersonEntity: Name: NameFull: Sandkuijl LA – PersonEntity: Name: NameFull: Terwindt GM – PersonEntity: Name: NameFull: Haan J – PersonEntity: Name: NameFull: van den Maagdenberg AM – PersonEntity: Name: NameFull: Jen J – PersonEntity: Name: NameFull: Baloh RW – PersonEntity: Name: NameFull: Barilla-LaBarca ML – PersonEntity: Name: NameFull: Saccone NL – PersonEntity: Name: NameFull: Atkinson JP – PersonEntity: Name: NameFull: Ferrari MD – PersonEntity: Name: NameFull: Freimer NB – PersonEntity: Name: NameFull: Frants RR IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 08 Text: 2001 Aug Type: published Y: 2001 Identifiers: – Type: issn-print Value: 0002-9297 Numbering: – Type: volume Value: 69 – Type: issue Value: 2 Titles: – TitleFull: American journal of human genetics Type: main |
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