PROMM and deafness: exclusion of ZNF9 as the disease gene in DFNA18 suggests a polygenic origin of the PROMM/DM2 phenotype.
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| Title: | PROMM and deafness: exclusion of ZNF9 as the disease gene in DFNA18 suggests a polygenic origin of the PROMM/DM2 phenotype. |
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| Authors: | Bonsch, D., Neumann, C., Lang-Roth, R., Witte, O., Lamprecht-Dinnesen, A., Deufel, T. |
| Source: | Clinical Genetics. Jan2003, Vol. 63 Issue 1, p73-75. 3p. |
| Database: | Academic Search Ultimate |
| FullText | Links: – Type: pdflink Text: Availability: 0 |
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| Header | DbId: asn DbLabel: Academic Search Ultimate An: 8739211 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: PROMM and deafness: exclusion of ZNF9 as the disease gene in DFNA18 suggests a polygenic origin of the PROMM/DM2 phenotype. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Bonsch%2C+D%2E%22">Bonsch, D.</searchLink><br /><searchLink fieldCode="AR" term="%22Neumann%2C+C%2E%22">Neumann, C.</searchLink><br /><searchLink fieldCode="AR" term="%22Lang-Roth%2C+R%2E%22">Lang-Roth, R.</searchLink><br /><searchLink fieldCode="AR" term="%22Witte%2C+O%2E%22">Witte, O.</searchLink><br /><searchLink fieldCode="AR" term="%22Lamprecht-Dinnesen%2C+A%2E%22">Lamprecht-Dinnesen, A.</searchLink><br /><searchLink fieldCode="AR" term="%22Deufel%2C+T%2E%22">Deufel, T.</searchLink> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22Clinical+Genetics%22">Clinical Genetics</searchLink>. Jan2003, Vol. 63 Issue 1, p73-75. 3p. |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=8739211 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1034/j.1399-0004.2003.630112.x Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 3 StartPage: 73 Titles: – TitleFull: PROMM and deafness: exclusion of ZNF9 as the disease gene in DFNA18 suggests a polygenic origin of the PROMM/DM2 phenotype. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Bonsch, D. – PersonEntity: Name: NameFull: Neumann, C. – PersonEntity: Name: NameFull: Lang-Roth, R. – PersonEntity: Name: NameFull: Witte, O. – PersonEntity: Name: NameFull: Lamprecht-Dinnesen, A. – PersonEntity: Name: NameFull: Deufel, T. IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 01 Text: Jan2003 Type: published Y: 2003 Identifiers: – Type: issn-print Value: 00099163 Numbering: – Type: volume Value: 63 – Type: issue Value: 1 Titles: – TitleFull: Clinical Genetics Type: main |
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