Identification of a deletion in the mismatch repair gene, MSH2, using mouse-human cell hybrids monosomal for chromosome 2.
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| Title: | Identification of a deletion in the mismatch repair gene, MSH2, using mouse-human cell hybrids monosomal for chromosome 2. |
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| Authors: | Pyatt RE; Department of Pathology, Ohio State University, Columbus, Ohio, USA. rpyatt@emory.edu, Nakagawa H, Hampel H, Sedra M, Fuchik MB, Comeras I, de la Chapelle A, Prior TW |
| Source: | Clinical genetics [Clin Genet] 2003 Mar; Vol. 63 (3), pp. 215-8. |
| Publication Type: | Journal Article; Research Support, U.S. Gov't, P.H.S. |
| Journal Info: | Publisher: Munksgaard Country of Publication: Denmark NLM ID: 0253664 Publication Model: Print Cited Medium: Print ISSN: 0009-9163 (Print) Linking ISSN: 00099163 NLM ISO Abbreviation: Clin Genet Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
| FullText | Links: – Type: pdflink Text: Availability: 0 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 12694232 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Identification of a deletion in the mismatch repair gene, MSH2, using mouse-human cell hybrids monosomal for chromosome 2. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Pyatt+RE%22">Pyatt RE</searchLink>; Department of Pathology, Ohio State University, Columbus, Ohio, USA. rpyatt@emory.edu<br /><searchLink fieldCode="AU" term="%22Nakagawa+H%22">Nakagawa H</searchLink><br /><searchLink fieldCode="AU" term="%22Hampel+H%22">Hampel H</searchLink><br /><searchLink fieldCode="AU" term="%22Sedra+M%22">Sedra M</searchLink><br /><searchLink fieldCode="AU" term="%22Fuchik+MB%22">Fuchik MB</searchLink><br /><searchLink fieldCode="AU" term="%22Comeras+I%22">Comeras I</searchLink><br /><searchLink fieldCode="AU" term="%22de+la+Chapelle+A%22">de la Chapelle A</searchLink><br /><searchLink fieldCode="AU" term="%22Prior+TW%22">Prior TW</searchLink> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%220253664%22">Clinical genetics</searchLink> [Clin Genet] 2003 Mar; Vol. 63 (3), pp. 215-8. – 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="%22Munksgaard%22">Munksgaard </searchLink><i>Country of Publication: </i>Denmark <i>NLM ID: </i>0253664 <i>Publication Model: </i>Print <i>Cited Medium: </i>Print <i>ISSN: </i>0009-9163 (Print) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2200099163%22">00099163 </searchLink><i>NLM ISO Abbreviation: </i>Clin Genet <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=12694232 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1034/j.1399-0004.2003.00040.x Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 215 Titles: – TitleFull: Identification of a deletion in the mismatch repair gene, MSH2, using mouse-human cell hybrids monosomal for chromosome 2. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Pyatt RE – PersonEntity: Name: NameFull: Nakagawa H – PersonEntity: Name: NameFull: Hampel H – PersonEntity: Name: NameFull: Sedra M – PersonEntity: Name: NameFull: Fuchik MB – PersonEntity: Name: NameFull: Comeras I – PersonEntity: Name: NameFull: de la Chapelle A – PersonEntity: Name: NameFull: Prior TW IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 03 Text: 2003 Mar Type: published Y: 2003 Identifiers: – Type: issn-print Value: 0009-9163 Numbering: – Type: volume Value: 63 – Type: issue Value: 3 Titles: – TitleFull: Clinical genetics Type: main |
| ResultId | 1 |
