View in EDS PDF Full Text

Expanding the phenotypic spectrum of ARID1B-mediated disorders and identification of altered cell-cycle dynamics due to ARID1B haploinsufficiency.

Saved in:
Bibliographic Details
Title: Expanding the phenotypic spectrum of ARID1B-mediated disorders and identification of altered cell-cycle dynamics due to ARID1B haploinsufficiency.
Authors: Sim JC, White SM, Fitzpatrick E, Wilson GR, Gillies G, Pope K, Mountford HS, Torring PM, McKee S, Vulto-van Silfhout AT, Jhangiani SN, Muzny DM, Leventer RJ, Delatycki MB, Amor DJ, Lockhart PJ; Bruce Lefroy Centre for Genetic Health Research, Murdoch Childrens Research Institute, Parkville, Victoria 3052, Australia. paul.lockhart@mcri.edu.au.
Source: Orphanet journal of rare diseases [Orphanet J Rare Dis] 2014 Mar 27; Vol. 9, pp. 43. Date of Electronic Publication: 2014 Mar 27.
Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
Journal Info: Publisher: BioMed Central Country of Publication: England NLM ID: 101266602 Publication Model: Electronic Cited Medium: Internet ISSN: 1750-1172 (Electronic) Linking ISSN: 17501172 NLM ISO Abbreviation: Orphanet J Rare Dis Subsets: MEDLINE
Database: MEDLINE Ultimate
FullText Links:
  – Type: pdflink
Text:
  Availability: 0
Header DbId: mdl
DbLabel: MEDLINE Ultimate
An: 24674232
AccessLevel: 2
PubType: Academic Journal
PubTypeId: academicJournal
PreciseRelevancyScore: 0
IllustrationInfo
Items – Name: Title
  Label: Title
  Group: Ti
  Data: Expanding the phenotypic spectrum of ARID1B-mediated disorders and identification of altered cell-cycle dynamics due to ARID1B haploinsufficiency.
– Name: Author
  Label: Authors
  Group: Au
  Data: <searchLink fieldCode="AU" term="%22Sim+JC%22">Sim JC</searchLink><br /><searchLink fieldCode="AU" term="%22White+SM%22">White SM</searchLink><br /><searchLink fieldCode="AU" term="%22Fitzpatrick+E%22">Fitzpatrick E</searchLink><br /><searchLink fieldCode="AU" term="%22Wilson+GR%22">Wilson GR</searchLink><br /><searchLink fieldCode="AU" term="%22Gillies+G%22">Gillies G</searchLink><br /><searchLink fieldCode="AU" term="%22Pope+K%22">Pope K</searchLink><br /><searchLink fieldCode="AU" term="%22Mountford+HS%22">Mountford HS</searchLink><br /><searchLink fieldCode="AU" term="%22Torring+PM%22">Torring PM</searchLink><br /><searchLink fieldCode="AU" term="%22McKee+S%22">McKee S</searchLink><br /><searchLink fieldCode="AU" term="%22Vulto-van+Silfhout+AT%22">Vulto-van Silfhout AT</searchLink><br /><searchLink fieldCode="AU" term="%22Jhangiani+SN%22">Jhangiani SN</searchLink><br /><searchLink fieldCode="AU" term="%22Muzny+DM%22">Muzny DM</searchLink><br /><searchLink fieldCode="AU" term="%22Leventer+RJ%22">Leventer RJ</searchLink><br /><searchLink fieldCode="AU" term="%22Delatycki+MB%22">Delatycki MB</searchLink><br /><searchLink fieldCode="AU" term="%22Amor+DJ%22">Amor DJ</searchLink><br /><searchLink fieldCode="AU" term="%22Lockhart+PJ%22">Lockhart PJ</searchLink>; Bruce Lefroy Centre for Genetic Health Research, Murdoch Childrens Research Institute, Parkville, Victoria 3052, Australia. paul.lockhart@mcri.edu.au.
– Name: TitleSource
  Label: Source
  Group: Src
  Data: <searchLink fieldCode="JN" term="%22101266602%22">Orphanet journal of rare diseases</searchLink> [Orphanet J Rare Dis] 2014 Mar 27; Vol. 9, pp. 43. <i>Date of Electronic Publication: </i>2014 Mar 27.
– Name: TypePub
  Label: Publication Type
  Group: TypPub
  Data: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
– Name: TitleSource
  Label: Journal Info
  Group: Src
  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22BioMed+Central%22">BioMed Central </searchLink><i>Country of Publication: </i>England <i>NLM ID: </i>101266602 <i>Publication Model: </i>Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1750-1172 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2217501172%22">17501172 </searchLink><i>NLM ISO Abbreviation: </i>Orphanet J Rare Dis <i>Subsets: </i>MEDLINE
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=24674232
RecordInfo BibRecord:
  BibEntity:
    Identifiers:
      – Type: doi
        Value: 10.1186/1750-1172-9-43
    Languages:
      – Code: eng
        Text: English
    PhysicalDescription:
      Pagination:
        StartPage: 43
    Titles:
      – TitleFull: Expanding the phenotypic spectrum of ARID1B-mediated disorders and identification of altered cell-cycle dynamics due to ARID1B haploinsufficiency.
        Type: main
  BibRelationships:
    HasContributorRelationships:
      – PersonEntity:
          Name:
            NameFull: Sim JC
      – PersonEntity:
          Name:
            NameFull: White SM
      – PersonEntity:
          Name:
            NameFull: Fitzpatrick E
      – PersonEntity:
          Name:
            NameFull: Wilson GR
      – PersonEntity:
          Name:
            NameFull: Gillies G
      – PersonEntity:
          Name:
            NameFull: Pope K
      – PersonEntity:
          Name:
            NameFull: Mountford HS
      – PersonEntity:
          Name:
            NameFull: Torring PM
      – PersonEntity:
          Name:
            NameFull: McKee S
      – PersonEntity:
          Name:
            NameFull: Vulto-van Silfhout AT
      – PersonEntity:
          Name:
            NameFull: Jhangiani SN
      – PersonEntity:
          Name:
            NameFull: Muzny DM
      – PersonEntity:
          Name:
            NameFull: Leventer RJ
      – PersonEntity:
          Name:
            NameFull: Delatycki MB
      – PersonEntity:
          Name:
            NameFull: Amor DJ
      – PersonEntity:
          Name:
            NameFull: Lockhart PJ
    IsPartOfRelationships:
      – BibEntity:
          Dates:
            – D: 27
              M: 03
              Text: 2014 Mar 27
              Type: published
              Y: 2014
          Identifiers:
            – Type: issn-electronic
              Value: 1750-1172
          Numbering:
            – Type: volume
              Value: 9
          Titles:
            – TitleFull: Orphanet journal of rare diseases
              Type: main
ResultId 1