Whole Exome Sequencing in Patients With Developmental Delay/Intellectual Disability (DD/ID), Epilepsy and the First Turkish Patient Diagnosed With BCL11A‐Related Intellectual Disability.

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Title: Whole Exome Sequencing in Patients With Developmental Delay/Intellectual Disability (DD/ID), Epilepsy and the First Turkish Patient Diagnosed With BCL11A‐Related Intellectual Disability.
Authors: Akkus, Nejmiye1 (AUTHOR) drnejmiyeakkus@gmail.com, Canbal, Abdullah2 (AUTHOR), Guneysu, Seda3 (AUTHOR), Gokce, Erkan4 (AUTHOR), Duzgun, Pakize5 (AUTHOR), Barıs, İbrahim6 (AUTHOR)
Source: Molecular Genetics & Genomic Medicine. Jan2026, Vol. 14 Issue 1, p1-16. 16p.
Database: Academic Search Ultimate
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  Data: Whole Exome Sequencing in Patients With Developmental Delay/Intellectual Disability (DD/ID), Epilepsy and the First Turkish Patient Diagnosed With BCL11A‐Related Intellectual Disability.
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  Data: <searchLink fieldCode="JN" term="%22Molecular+Genetics+%26+Genomic+Medicine%22">Molecular Genetics & Genomic Medicine</searchLink>. Jan2026, Vol. 14 Issue 1, p1-16. 16p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=191104402
RecordInfo BibRecord:
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      – Type: doi
        Value: 10.1002/mgg3.70180
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      – Code: eng
        Text: English
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        PageCount: 16
        StartPage: 1
    Titles:
      – TitleFull: Whole Exome Sequencing in Patients With Developmental Delay/Intellectual Disability (DD/ID), Epilepsy and the First Turkish Patient Diagnosed With BCL11A‐Related Intellectual Disability.
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          Name:
            NameFull: Akkus, Nejmiye
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            NameFull: Canbal, Abdullah
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            NameFull: Guneysu, Seda
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            NameFull: Gokce, Erkan
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            NameFull: Duzgun, Pakize
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            NameFull: Barıs, İbrahim
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            – D: 01
              M: 01
              Text: Jan2026
              Type: published
              Y: 2026
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              Value: 14
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