View in EDS HTML Full Text PDF Full Text

A Novel De Novo STAG1 Variant in Monozygotic Twins with Neurodevelopmental Disorder: New Insights in Clinical Heterogeneity.

Saved in:
Bibliographic Details
Title: A Novel De Novo STAG1 Variant in Monozygotic Twins with Neurodevelopmental Disorder: New Insights in Clinical Heterogeneity.
Authors: Cipriano L; Department of Molecular Medicine and Medical Biotechnology, University Federico II, 80131 Naples, Italy., Russo R; Department of Molecular Medicine and Medical Biotechnology, University Federico II, 80131 Naples, Italy.; CEINGE Biotecnologie Avanzate Franco Salvatore, 80145 Naples, Italy., Andolfo I; Department of Molecular Medicine and Medical Biotechnology, University Federico II, 80131 Naples, Italy.; CEINGE Biotecnologie Avanzate Franco Salvatore, 80145 Naples, Italy., Manno M; Department of Molecular Medicine and Medical Biotechnology, University Federico II, 80131 Naples, Italy.; CEINGE Biotecnologie Avanzate Franco Salvatore, 80145 Naples, Italy., Piscopo R; Department of Neuroscience, Reproductive and Odontostomatological Sciences, University Federico II, 80131 Naples, Italy., Iolascon A; Department of Molecular Medicine and Medical Biotechnology, University Federico II, 80131 Naples, Italy.; CEINGE Biotecnologie Avanzate Franco Salvatore, 80145 Naples, Italy., Piscopo C; Medical and Laboratory Genetics Unit, A.O.R.N. 'Antonio Cardarelli', 80131 Naples, Italy.
Source: Genes [Genes (Basel)] 2024 Sep 09; Vol. 15 (9). Date of Electronic Publication: 2024 Sep 09.
Publication Type: Case Reports; Journal Article
Journal Info: Publisher: MDPI Country of Publication: Switzerland NLM ID: 101551097 Publication Model: Electronic Cited Medium: Internet ISSN: 2073-4425 (Electronic) Linking ISSN: 20734425 NLM ISO Abbreviation: Genes (Basel) 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: 39336775
AccessLevel: 2
PubType: Academic Journal
PubTypeId: academicJournal
PreciseRelevancyScore: 0
IllustrationInfo
Items – Name: Title
  Label: Title
  Group: Ti
  Data: A Novel De Novo STAG1 Variant in Monozygotic Twins with Neurodevelopmental Disorder: New Insights in Clinical Heterogeneity.
– Name: Author
  Label: Authors
  Group: Au
  Data: <searchLink fieldCode="AU" term="%22Cipriano+L%22">Cipriano L</searchLink>; Department of Molecular Medicine and Medical Biotechnology, University Federico II, 80131 Naples, Italy.<br /><searchLink fieldCode="AU" term="%22Russo+R%22">Russo R</searchLink>; Department of Molecular Medicine and Medical Biotechnology, University Federico II, 80131 Naples, Italy.; CEINGE Biotecnologie Avanzate Franco Salvatore, 80145 Naples, Italy.<br /><searchLink fieldCode="AU" term="%22Andolfo+I%22">Andolfo I</searchLink>; Department of Molecular Medicine and Medical Biotechnology, University Federico II, 80131 Naples, Italy.; CEINGE Biotecnologie Avanzate Franco Salvatore, 80145 Naples, Italy.<br /><searchLink fieldCode="AU" term="%22Manno+M%22">Manno M</searchLink>; Department of Molecular Medicine and Medical Biotechnology, University Federico II, 80131 Naples, Italy.; CEINGE Biotecnologie Avanzate Franco Salvatore, 80145 Naples, Italy.<br /><searchLink fieldCode="AU" term="%22Piscopo+R%22">Piscopo R</searchLink>; Department of Neuroscience, Reproductive and Odontostomatological Sciences, University Federico II, 80131 Naples, Italy.<br /><searchLink fieldCode="AU" term="%22Iolascon+A%22">Iolascon A</searchLink>; Department of Molecular Medicine and Medical Biotechnology, University Federico II, 80131 Naples, Italy.; CEINGE Biotecnologie Avanzate Franco Salvatore, 80145 Naples, Italy.<br /><searchLink fieldCode="AU" term="%22Piscopo+C%22">Piscopo C</searchLink>; Medical and Laboratory Genetics Unit, A.O.R.N. 'Antonio Cardarelli', 80131 Naples, Italy.
– Name: TitleSource
  Label: Source
  Group: Src
  Data: <searchLink fieldCode="JN" term="%22101551097%22">Genes</searchLink> [Genes (Basel)] 2024 Sep 09; Vol. 15 (9). <i>Date of Electronic Publication: </i>2024 Sep 09.
– 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="%22MDPI%22">MDPI </searchLink><i>Country of Publication: </i>Switzerland <i>NLM ID: </i>101551097 <i>Publication Model: </i>Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>2073-4425 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2220734425%22">20734425 </searchLink><i>NLM ISO Abbreviation: </i>Genes (Basel) <i>Subsets: </i>MEDLINE
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=39336775
RecordInfo BibRecord:
  BibEntity:
    Identifiers:
      – Type: doi
        Value: 10.3390/genes15091184
    Languages:
      – Code: eng
        Text: English
    Titles:
      – TitleFull: A Novel De Novo STAG1 Variant in Monozygotic Twins with Neurodevelopmental Disorder: New Insights in Clinical Heterogeneity.
        Type: main
  BibRelationships:
    HasContributorRelationships:
      – PersonEntity:
          Name:
            NameFull: Cipriano L
      – PersonEntity:
          Name:
            NameFull: Russo R
      – PersonEntity:
          Name:
            NameFull: Andolfo I
      – PersonEntity:
          Name:
            NameFull: Manno M
      – PersonEntity:
          Name:
            NameFull: Piscopo R
      – PersonEntity:
          Name:
            NameFull: Iolascon A
      – PersonEntity:
          Name:
            NameFull: Piscopo C
    IsPartOfRelationships:
      – BibEntity:
          Dates:
            – D: 09
              M: 09
              Text: 2024 Sep 09
              Type: published
              Y: 2024
          Identifiers:
            – Type: issn-electronic
              Value: 2073-4425
          Numbering:
            – Type: volume
              Value: 15
            – Type: issue
              Value: 9
          Titles:
            – TitleFull: Genes
              Type: main
ResultId 1