Extension of the clinical and molecular phenotype of DIAPH1-associated autosomal dominant hearing loss ( DFNA1).
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| Title: | Extension of the clinical and molecular phenotype of DIAPH1-associated autosomal dominant hearing loss ( DFNA1). |
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| Authors: | Neuhaus, C.1, Lang‐Roth, R.2, Zimmermann, U.3, Heller, R.4, Eisenberger, T.1, Weikert, M.5, Markus, S.6, Knipper, M.2, Bolz, H.J.1,4 hanno.bolz@bioscientia.de |
| Source: | Clinical Genetics. Jun2017, Vol. 91 Issue 6, p892-901. 11p. 2 Color Photographs, 2 Diagrams, 2 Charts, 1 Graph. |
| Database: | Academic Search Ultimate |
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| FullText | Links: – Type: pdflink Text: Availability: 1 |
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| Header | DbId: asn DbLabel: Academic Search Ultimate An: 123283081 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Extension of the clinical and molecular phenotype of DIAPH1-associated autosomal dominant hearing loss ( DFNA1). – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Neuhaus%2C+C%2E%22">Neuhaus, C.</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Lang‐Roth%2C+R%2E%22">Lang‐Roth, R.</searchLink><relatesTo>2</relatesTo><br /><searchLink fieldCode="AR" term="%22Zimmermann%2C+U%2E%22">Zimmermann, U.</searchLink><relatesTo>3</relatesTo><br /><searchLink fieldCode="AR" term="%22Heller%2C+R%2E%22">Heller, R.</searchLink><relatesTo>4</relatesTo><br /><searchLink fieldCode="AR" term="%22Eisenberger%2C+T%2E%22">Eisenberger, T.</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Weikert%2C+M%2E%22">Weikert, M.</searchLink><relatesTo>5</relatesTo><br /><searchLink fieldCode="AR" term="%22Markus%2C+S%2E%22">Markus, S.</searchLink><relatesTo>6</relatesTo><br /><searchLink fieldCode="AR" term="%22Knipper%2C+M%2E%22">Knipper, M.</searchLink><relatesTo>2</relatesTo><br /><searchLink fieldCode="AR" term="%22Bolz%2C+H%2EJ%2E%22">Bolz, H.J.</searchLink><relatesTo>1,4</relatesTo><i> hanno.bolz@bioscientia.de</i> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22Clinical+Genetics%22">Clinical Genetics</searchLink>. Jun2017, Vol. 91 Issue 6, p892-901. 11p. 2 Color Photographs, 2 Diagrams, 2 Charts, 1 Graph. |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=123283081 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1111/cge.12915 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 11 StartPage: 892 Titles: – TitleFull: Extension of the clinical and molecular phenotype of DIAPH1-associated autosomal dominant hearing loss ( DFNA1). Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Neuhaus, C. – PersonEntity: Name: NameFull: Lang‐Roth, R. – PersonEntity: Name: NameFull: Zimmermann, U. – PersonEntity: Name: NameFull: Heller, R. – PersonEntity: Name: NameFull: Eisenberger, T. – PersonEntity: Name: NameFull: Weikert, M. – PersonEntity: Name: NameFull: Markus, S. – PersonEntity: Name: NameFull: Knipper, M. – PersonEntity: Name: NameFull: Bolz, H.J. IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 06 Text: Jun2017 Type: published Y: 2017 Identifiers: – Type: issn-print Value: 00099163 Numbering: – Type: volume Value: 91 – Type: issue Value: 6 Titles: – TitleFull: Clinical Genetics Type: main |
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