A novel de novo variant in the RUNX2 gene causes cleidocranial dysplasia in a Malian girl.
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| Title: | A novel de novo variant in the RUNX2 gene causes cleidocranial dysplasia in a Malian girl. |
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| 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 |
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| Header | DbId: asn DbLabel: Academic Search Ultimate An: 175751186 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| 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 |
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