A novel de novo variant in the RUNX2 gene causes cleidocranial dysplasia in a Malian girl.

Saved in:
Bibliographic Details
Title: A novel de novo variant in the RUNX2 gene causes cleidocranial dysplasia in a Malian girl.
Authors: Cissé, Lassana1 (AUTHOR) lassciss@gmail.com, Yalcouyé, Abdoulaye2 (AUTHOR), Touré, Kadidia Oumar2,3 (AUTHOR), Coulibaly, Youlouza4 (AUTHOR), Maiga, Alassane Baneye2 (AUTHOR), Bamba, Salia2 (AUTHOR), Diallo, Dramane5 (AUTHOR), Diarra, Salimata2,6 (AUTHOR), Taméga, Abdoulaye2 (AUTHOR), Traoré, Oumou2 (AUTHOR), Kotioumbé, Mahamadou2 (AUTHOR), Sangaré, Moussa Aly2 (AUTHOR), Ba, Hamidou Oumar2,7 (AUTHOR), Simaga, Assiatou2,8 (AUTHOR), Koné, Fatogoma Issa2,9 (AUTHOR), Samassekou, Oumar2 (AUTHOR), Koné, Amadou2,5 (AUTHOR), Guinto, Cheick Oumar1,2 (AUTHOR), Landouré, Guida1,2 (AUTHOR)
Source: Clinical Case Reports. Feb2024, Vol. 12 Issue 2, p1-6. 6p.
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: 175751186
AccessLevel: 2
PubType: Academic Journal
PubTypeId: academicJournal
PreciseRelevancyScore: 0
IllustrationInfo
Items – Name: Title
  Label: Title
  Group: Ti
  Data: A novel de novo variant in the RUNX2 gene causes cleidocranial dysplasia in a Malian girl.
– Name: Author
  Label: Authors
  Group: Au
  Data: <searchLink fieldCode="AR" term="%22Cissé%2C+Lassana%22">Cissé, Lassana</searchLink><relatesTo>1</relatesTo> (AUTHOR)<i> lassciss@gmail.com</i><br /><searchLink fieldCode="AR" term="%22Yalcouyé%2C+Abdoulaye%22">Yalcouyé, Abdoulaye</searchLink><relatesTo>2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Touré%2C+Kadidia+Oumar%22">Touré, Kadidia Oumar</searchLink><relatesTo>2,3</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Coulibaly%2C+Youlouza%22">Coulibaly, Youlouza</searchLink><relatesTo>4</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Maiga%2C+Alassane+Baneye%22">Maiga, Alassane Baneye</searchLink><relatesTo>2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Bamba%2C+Salia%22">Bamba, Salia</searchLink><relatesTo>2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Diallo%2C+Dramane%22">Diallo, Dramane</searchLink><relatesTo>5</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Diarra%2C+Salimata%22">Diarra, Salimata</searchLink><relatesTo>2,6</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Taméga%2C+Abdoulaye%22">Taméga, Abdoulaye</searchLink><relatesTo>2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Traoré%2C+Oumou%22">Traoré, Oumou</searchLink><relatesTo>2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Kotioumbé%2C+Mahamadou%22">Kotioumbé, Mahamadou</searchLink><relatesTo>2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Sangaré%2C+Moussa+Aly%22">Sangaré, Moussa Aly</searchLink><relatesTo>2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Ba%2C+Hamidou+Oumar%22">Ba, Hamidou Oumar</searchLink><relatesTo>2,7</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Simaga%2C+Assiatou%22">Simaga, Assiatou</searchLink><relatesTo>2,8</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Koné%2C+Fatogoma+Issa%22">Koné, Fatogoma Issa</searchLink><relatesTo>2,9</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Samassekou%2C+Oumar%22">Samassekou, Oumar</searchLink><relatesTo>2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Koné%2C+Amadou%22">Koné, Amadou</searchLink><relatesTo>2,5</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Guinto%2C+Cheick+Oumar%22">Guinto, Cheick Oumar</searchLink><relatesTo>1,2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Landouré%2C+Guida%22">Landouré, Guida</searchLink><relatesTo>1,2</relatesTo> (AUTHOR)
– Name: TitleSource
  Label: Source
  Group: Src
  Data: <searchLink fieldCode="JN" term="%22Clinical+Case+Reports%22">Clinical Case Reports</searchLink>. Feb2024, Vol. 12 Issue 2, p1-6. 6p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=175751186
RecordInfo BibRecord:
  BibEntity:
    Identifiers:
      – Type: doi
        Value: 10.1002/ccr3.8551
    Languages:
      – Code: eng
        Text: English
    PhysicalDescription:
      Pagination:
        PageCount: 6
        StartPage: 1
    Titles:
      – TitleFull: A novel de novo variant in the RUNX2 gene causes cleidocranial dysplasia in a Malian girl.
        Type: main
  BibRelationships:
    HasContributorRelationships:
      – PersonEntity:
          Name:
            NameFull: Cissé, Lassana
      – PersonEntity:
          Name:
            NameFull: Yalcouyé, Abdoulaye
      – PersonEntity:
          Name:
            NameFull: Touré, Kadidia Oumar
      – PersonEntity:
          Name:
            NameFull: Coulibaly, Youlouza
      – PersonEntity:
          Name:
            NameFull: Maiga, Alassane Baneye
      – PersonEntity:
          Name:
            NameFull: Bamba, Salia
      – PersonEntity:
          Name:
            NameFull: Diallo, Dramane
      – PersonEntity:
          Name:
            NameFull: Diarra, Salimata
      – PersonEntity:
          Name:
            NameFull: Taméga, Abdoulaye
      – PersonEntity:
          Name:
            NameFull: Traoré, Oumou
      – PersonEntity:
          Name:
            NameFull: Kotioumbé, Mahamadou
      – PersonEntity:
          Name:
            NameFull: Sangaré, Moussa Aly
      – PersonEntity:
          Name:
            NameFull: Ba, Hamidou Oumar
      – PersonEntity:
          Name:
            NameFull: Simaga, Assiatou
      – PersonEntity:
          Name:
            NameFull: Koné, Fatogoma Issa
      – PersonEntity:
          Name:
            NameFull: Samassekou, Oumar
      – PersonEntity:
          Name:
            NameFull: Koné, Amadou
      – PersonEntity:
          Name:
            NameFull: Guinto, Cheick Oumar
      – PersonEntity:
          Name:
            NameFull: Landouré, Guida
    IsPartOfRelationships:
      – BibEntity:
          Dates:
            – D: 01
              M: 02
              Text: Feb2024
              Type: published
              Y: 2024
          Identifiers:
            – Type: issn-print
              Value: 20500904
          Numbering:
            – Type: volume
              Value: 12
            – Type: issue
              Value: 2
          Titles:
            – TitleFull: Clinical Case Reports
              Type: main
ResultId 1