View in EDS HTML Full Text PDF Full Text

Menkes disease complicated by concurrent Koolen-de Vries syndrome (17q21.31 deletion).

Saved in:
Bibliographic Details
Title: Menkes disease complicated by concurrent Koolen-de Vries syndrome (17q21.31 deletion).
Authors: Woodfin T; Department of Pediatrics, University of Alabama at Birmingham, Birmingham, Alabama., Stoops C; Department of Pediatrics, University of Alabama at Birmingham, Birmingham, Alabama., Philips JB 3rd; Department of Pediatrics, University of Alabama at Birmingham, Birmingham, Alabama., Lose E; Department of Pediatrics, University of Alabama at Birmingham, Birmingham, Alabama., Mikhail FM; Department of Genetics, University of Alabama at Birmingham, Birmingham, Alabama., Hurst A; Department of Genetics, University of Alabama at Birmingham, Birmingham, Alabama.
Source: Molecular genetics & genomic medicine [Mol Genet Genomic Med] 2019 Aug; Vol. 7 (8), pp. e829. Date of Electronic Publication: 2019 Jun 28.
Publication Type: Case Reports; Journal Article
Journal Info: Publisher: John Wiley & Sons Country of Publication: United States NLM ID: 101603758 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2324-9269 (Electronic) Linking ISSN: 23249269 NLM ISO Abbreviation: Mol Genet Genomic Med Subsets: MEDLINE
Database: MEDLINE Ultimate
Full text is not displayed to guests.
FullText Links:
  – Type: pdflink
Text:
  Availability: 1
Header DbId: mdl
DbLabel: MEDLINE Ultimate
An: 31250568
AccessLevel: 2
PubType: Academic Journal
PubTypeId: academicJournal
PreciseRelevancyScore: 0
IllustrationInfo
Items – Name: Title
  Label: Title
  Group: Ti
  Data: Menkes disease complicated by concurrent Koolen-de Vries syndrome (17q21.31 deletion).
– Name: Author
  Label: Authors
  Group: Au
  Data: <searchLink fieldCode="AU" term="%22Woodfin+T%22">Woodfin T</searchLink>; Department of Pediatrics, University of Alabama at Birmingham, Birmingham, Alabama.<br /><searchLink fieldCode="AU" term="%22Stoops+C%22">Stoops C</searchLink>; Department of Pediatrics, University of Alabama at Birmingham, Birmingham, Alabama.<br /><searchLink fieldCode="AU" term="%22Philips+JB+3rd%22">Philips JB 3rd</searchLink>; Department of Pediatrics, University of Alabama at Birmingham, Birmingham, Alabama.<br /><searchLink fieldCode="AU" term="%22Lose+E%22">Lose E</searchLink>; Department of Pediatrics, University of Alabama at Birmingham, Birmingham, Alabama.<br /><searchLink fieldCode="AU" term="%22Mikhail+FM%22">Mikhail FM</searchLink>; Department of Genetics, University of Alabama at Birmingham, Birmingham, Alabama.<br /><searchLink fieldCode="AU" term="%22Hurst+A%22">Hurst A</searchLink>; Department of Genetics, University of Alabama at Birmingham, Birmingham, Alabama.
– Name: TitleSource
  Label: Source
  Group: Src
  Data: <searchLink fieldCode="JN" term="%22101603758%22">Molecular genetics & genomic medicine</searchLink> [Mol Genet Genomic Med] 2019 Aug; Vol. 7 (8), pp. e829. <i>Date of Electronic Publication: </i>2019 Jun 28.
– Name: TypePub
  Label: Publication Type
  Group: TypPub
  Data: Case Reports; Journal Article
– Name: TitleSource
  Label: Journal Info
  Group: Src
  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22John+Wiley+%26+Sons%22">John Wiley & Sons </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>101603758 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>2324-9269 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2223249269%22">23249269 </searchLink><i>NLM ISO Abbreviation: </i>Mol Genet Genomic Med <i>Subsets: </i>MEDLINE
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=31250568
RecordInfo BibRecord:
  BibEntity:
    Identifiers:
      – Type: doi
        Value: 10.1002/mgg3.829
    Languages:
      – Code: eng
        Text: English
    PhysicalDescription:
      Pagination:
        StartPage: e829
    Titles:
      – TitleFull: Menkes disease complicated by concurrent Koolen-de Vries syndrome (17q21.31 deletion).
        Type: main
  BibRelationships:
    HasContributorRelationships:
      – PersonEntity:
          Name:
            NameFull: Woodfin T
      – PersonEntity:
          Name:
            NameFull: Stoops C
      – PersonEntity:
          Name:
            NameFull: Philips JB 3rd
      – PersonEntity:
          Name:
            NameFull: Lose E
      – PersonEntity:
          Name:
            NameFull: Mikhail FM
      – PersonEntity:
          Name:
            NameFull: Hurst A
    IsPartOfRelationships:
      – BibEntity:
          Dates:
            – D: 01
              M: 08
              Text: 2019 Aug
              Type: published
              Y: 2019
          Identifiers:
            – Type: issn-electronic
              Value: 2324-9269
          Numbering:
            – Type: volume
              Value: 7
            – Type: issue
              Value: 8
          Titles:
            – TitleFull: Molecular genetics & genomic medicine
              Type: main
ResultId 1