Severe cognitive impairment in DMD: obvious clinical indication for Dp71 isoform point mutation screening.
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| Title: | Severe cognitive impairment in DMD: obvious clinical indication for Dp71 isoform point mutation screening. |
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| Authors: | Moizard MP; Unité de Génétique, Hôpital Bretonneau, Tours, France. moizard-m@lemel.fr, Toutain A, Fournier D, Berret F, Raynaud M, Billard C, Andres C, Moraine C |
| Source: | European journal of human genetics : EJHG [Eur J Hum Genet] 2000 Jul; Vol. 8 (7), pp. 552-6. |
| Publication Type: | Journal Article; Research Support, Non-U.S. Gov't |
| Journal Info: | Publisher: Nature Publishing Group Country of Publication: England NLM ID: 9302235 Publication Model: Print Cited Medium: Print ISSN: 1018-4813 (Print) Linking ISSN: 10184813 NLM ISO Abbreviation: Eur J Hum Genet Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
| FullText | Links: – Type: pdflink Text: Availability: 0 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 10909857 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Severe cognitive impairment in DMD: obvious clinical indication for Dp71 isoform point mutation screening. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Moizard+MP%22">Moizard MP</searchLink>; Unité de Génétique, Hôpital Bretonneau, Tours, France. moizard-m@lemel.fr<br /><searchLink fieldCode="AU" term="%22Toutain+A%22">Toutain A</searchLink><br /><searchLink fieldCode="AU" term="%22Fournier+D%22">Fournier D</searchLink><br /><searchLink fieldCode="AU" term="%22Berret+F%22">Berret F</searchLink><br /><searchLink fieldCode="AU" term="%22Raynaud+M%22">Raynaud M</searchLink><br /><searchLink fieldCode="AU" term="%22Billard+C%22">Billard C</searchLink><br /><searchLink fieldCode="AU" term="%22Andres+C%22">Andres C</searchLink><br /><searchLink fieldCode="AU" term="%22Moraine+C%22">Moraine C</searchLink> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%229302235%22">European journal of human genetics : EJHG</searchLink> [Eur J Hum Genet] 2000 Jul; Vol. 8 (7), pp. 552-6. – Name: TypePub Label: Publication Type Group: TypPub Data: Journal Article; Research Support, Non-U.S. Gov't – Name: TitleSource Label: Journal Info Group: Src Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Nature+Publishing+Group%22">Nature Publishing Group </searchLink><i>Country of Publication: </i>England <i>NLM ID: </i>9302235 <i>Publication Model: </i>Print <i>Cited Medium: </i>Print <i>ISSN: </i>1018-4813 (Print) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2210184813%22">10184813 </searchLink><i>NLM ISO Abbreviation: </i>Eur J Hum Genet <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=10909857 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1038/sj.ejhg.5200488 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 552 Titles: – TitleFull: Severe cognitive impairment in DMD: obvious clinical indication for Dp71 isoform point mutation screening. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Moizard MP – PersonEntity: Name: NameFull: Toutain A – PersonEntity: Name: NameFull: Fournier D – PersonEntity: Name: NameFull: Berret F – PersonEntity: Name: NameFull: Raynaud M – PersonEntity: Name: NameFull: Billard C – PersonEntity: Name: NameFull: Andres C – PersonEntity: Name: NameFull: Moraine C IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 07 Text: 2000 Jul Type: published Y: 2000 Identifiers: – Type: issn-print Value: 1018-4813 Numbering: – Type: volume Value: 8 – Type: issue Value: 7 Titles: – TitleFull: European journal of human genetics : EJHG Type: main |
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