Neuronal Heterotopy in a Patient with Wiedemann–Steiner Syndrome Caused by a Truncating KMT2A Variant: Clinical and Genetic Correlations.

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Title: Neuronal Heterotopy in a Patient with Wiedemann–Steiner Syndrome Caused by a Truncating KMT2A Variant: Clinical and Genetic Correlations.
Authors: Sokolova, Teodora1 (AUTHOR) iglika.sotkova@mu-plovdiv.bg, Ivanov, Hristo1,2 (AUTHOR) vili.stoyanova@mu-plovdiv.bg, Panova, Margarita1,2 (AUTHOR), Sotkova-Ivanova, Iglika1,2 (AUTHOR), Stoyanova, Vili1 (AUTHOR)
Source: Reports (MDPI AG). Mar2026, Vol. 9 Issue 1, p37. 11p.
Database: Academic Search Ultimate
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  Data: Neuronal Heterotopy in a Patient with Wiedemann–Steiner Syndrome Caused by a Truncating KMT2A Variant: Clinical and Genetic Correlations.
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  Data: <searchLink fieldCode="JN" term="%22Reports+%28MDPI+AG%29%22">Reports (MDPI AG)</searchLink>. Mar2026, Vol. 9 Issue 1, p37. 11p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=192664321
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        Value: 10.3390/reports9010037
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      – Code: eng
        Text: English
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        PageCount: 11
        StartPage: 37
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      – TitleFull: Neuronal Heterotopy in a Patient with Wiedemann–Steiner Syndrome Caused by a Truncating KMT2A Variant: Clinical and Genetic Correlations.
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            NameFull: Sokolova, Teodora
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            NameFull: Ivanov, Hristo
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            NameFull: Panova, Margarita
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            NameFull: Sotkova-Ivanova, Iglika
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            – D: 01
              M: 03
              Text: Mar2026
              Type: published
              Y: 2026
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