Using Whole Exome Sequencing to Identify Genetic Causes of Neurodevelopmental Disorders in a Cohort of 11 Patients: A Single Center Experience.
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| Title: | Using Whole Exome Sequencing to Identify Genetic Causes of Neurodevelopmental Disorders in a Cohort of 11 Patients: A Single Center Experience. |
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| Authors: | Tompa, Marton1,2 (AUTHOR), Sinko, Gabriella2 (AUTHOR), Mally, Judit3 (AUTHOR), Karteszi, Judit4 (AUTHOR), Kalman, Bernadette1,2,5 (AUTHOR) bernadette.kalman@pte.hu |
| Source: | International Journal of Molecular Sciences. Oct2025, Vol. 26 Issue 20, p10176. 17p. |
| Database: | Academic Search Ultimate |
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| FullText | Links: – Type: pdflink Text: Availability: 1 |
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| Header | DbId: asn DbLabel: Academic Search Ultimate An: 188956274 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=188956274 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.3390/ijms262010176 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 17 StartPage: 10176 Titles: – TitleFull: Using Whole Exome Sequencing to Identify Genetic Causes of Neurodevelopmental Disorders in a Cohort of 11 Patients: A Single Center Experience. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Tompa, Marton – PersonEntity: Name: NameFull: Sinko, Gabriella – PersonEntity: Name: NameFull: Mally, Judit – PersonEntity: Name: NameFull: Karteszi, Judit – PersonEntity: Name: NameFull: Kalman, Bernadette IsPartOfRelationships: – BibEntity: Dates: – D: 15 M: 10 Text: Oct2025 Type: published Y: 2025 Identifiers: – Type: issn-print Value: 16616596 Numbering: – Type: volume Value: 26 – Type: issue Value: 20 Titles: – TitleFull: International Journal of Molecular Sciences Type: main |
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