Extension of the clinical and molecular phenotype of DIAPH1-associated autosomal dominant hearing loss ( DFNA1).

Saved in:
Bibliographic Details
Title: Extension of the clinical and molecular phenotype of DIAPH1-associated autosomal dominant hearing loss ( DFNA1).
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
Full text is not displayed to guests.
FullText Links:
  – Type: pdflink
Text:
  Availability: 1
Header DbId: asn
DbLabel: Academic Search Ultimate
An: 123283081
AccessLevel: 2
PubType: Academic Journal
PubTypeId: academicJournal
PreciseRelevancyScore: 0
IllustrationInfo
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
ResultId 1