Case report: 7p22.3 deletion and 8q24.3 duplication in a patient with epilepsy and psychomotor delay-Does both possibly act to modulate a candidate gene region for the patient’s phenotype? R.
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| Title: | Case report: 7p22.3 deletion and 8q24.3 duplication in a patient with epilepsy and psychomotor delay-Does both possibly act to modulate a candidate gene region for the patient’s phenotype? R. |
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| Authors: | Touhami, Rahma, Foddha, Hajer, Alix, Eudeline, Jalloul, Afef, Mougou-Zerelli, Soumaya, Saad, Ali, Sanlaville, Damien, Khelil, Amel Haj |
| Source: | Frontiers in genetics 1/9/2023; Vol. 13. |
| Journal Info: | Publisher: Frontiers Media S.A. ISSN: 1664-8021 |
| Database: | MEDLINE Ultimate |
| FullText | Links: – Type: pdflink Text: Availability: 0 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: EPTOC163183345 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Case report: 7p22.3 deletion and 8q24.3 duplication in a patient with epilepsy and psychomotor delay-Does both possibly act to modulate a candidate gene region for the patient’s phenotype? R. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Touhami%2C+Rahma%22">Touhami, Rahma</searchLink><br /><searchLink fieldCode="AU" term="%22Foddha%2C+Hajer%22">Foddha, Hajer</searchLink><br /><searchLink fieldCode="AU" term="%22Alix%2C+Eudeline%22">Alix, Eudeline</searchLink><br /><searchLink fieldCode="AU" term="%22Jalloul%2C+Afef%22">Jalloul, Afef</searchLink><br /><searchLink fieldCode="AU" term="%22Mougou-Zerelli%2C+Soumaya%22">Mougou-Zerelli, Soumaya</searchLink><br /><searchLink fieldCode="AU" term="%22Saad%2C+Ali%22">Saad, Ali</searchLink><br /><searchLink fieldCode="AU" term="%22Sanlaville%2C+Damien%22">Sanlaville, Damien</searchLink><br /><searchLink fieldCode="AU" term="%22Khelil%2C+Amel+Haj%22">Khelil, Amel Haj</searchLink> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22101560621%22">Frontiers in genetics</searchLink> 1/9/2023; Vol. 13. – Name: TitleSource Label: Journal Info Group: Src Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Frontiers+Media+S%2EA%2E%22">Frontiers Media S.A. </searchLink><i>ISSN: </i>1664-8021 |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=EPTOC163183345 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.3389/fgene.2022.1061539 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 1 Titles: – TitleFull: Case report: 7p22.3 deletion and 8q24.3 duplication in a patient with epilepsy and psychomotor delay-Does both possibly act to modulate a candidate gene region for the patient’s phenotype? R. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Touhami, Rahma – PersonEntity: Name: NameFull: Foddha, Hajer – PersonEntity: Name: NameFull: Alix, Eudeline – PersonEntity: Name: NameFull: Jalloul, Afef – PersonEntity: Name: NameFull: Mougou-Zerelli, Soumaya – PersonEntity: Name: NameFull: Saad, Ali – PersonEntity: Name: NameFull: Sanlaville, Damien – PersonEntity: Name: NameFull: Khelil, Amel Haj IsPartOfRelationships: – BibEntity: Dates: – D: 09 M: 01 Text: 1/9/2023 Type: published Y: 2023 Identifiers: – Type: issn-print Value: 1664-8021 Numbering: – Type: volume Value: 13 Titles: – TitleFull: Frontiers in genetics Type: main |
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