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Double Genetic Diagnosis Involving MECP2 and EPHB4 in a Child with Neurodevelopmental Delay and Vascular Anomalies: A Case Report.

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Title: Double Genetic Diagnosis Involving MECP2 and EPHB4 in a Child with Neurodevelopmental Delay and Vascular Anomalies: A Case Report.
Authors: Sanri A; Department of Pediatric Genetics, Samsun Training and Research Hospital, Samsun, Turkey., Mutlu MB; Detagen Genetic Diseases Evaluation Center, Kayseri, Turkey.
Source: Molecular syndromology [Mol Syndromol] 2025 Oct 23. Date of Electronic Publication: 2025 Oct 23.
Publication Type: Journal Article
Journal Info: Publisher: S. Karger Country of Publication: Switzerland NLM ID: 101525192 Publication Model: Print-Electronic Cited Medium: Print ISSN: 1661-8769 (Print) Linking ISSN: 16618769 NLM ISO Abbreviation: Mol Syndromol
Database: MEDLINE Ultimate
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PubType: Academic Journal
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  Data: Double Genetic Diagnosis Involving MECP2 and EPHB4 in a Child with Neurodevelopmental Delay and Vascular Anomalies: A Case Report.
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  Data: <searchLink fieldCode="AU" term="%22Sanri+A%22">Sanri A</searchLink>; Department of Pediatric Genetics, Samsun Training and Research Hospital, Samsun, Turkey.<br /><searchLink fieldCode="AU" term="%22Mutlu+MB%22">Mutlu MB</searchLink>; Detagen Genetic Diseases Evaluation Center, Kayseri, Turkey.
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22S%2E+Karger%22">S. Karger </searchLink><i>Country of Publication: </i>Switzerland <i>NLM ID: </i>101525192 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Print <i>ISSN: </i>1661-8769 (Print) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2216618769%22">16618769 </searchLink><i>NLM ISO Abbreviation: </i>Mol Syndromol
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=41409310
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      – Type: doi
        Value: 10.1159/000549131
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      – Code: eng
        Text: English
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      – TitleFull: Double Genetic Diagnosis Involving MECP2 and EPHB4 in a Child with Neurodevelopmental Delay and Vascular Anomalies: A Case Report.
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            NameFull: Sanri A
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            NameFull: Mutlu MB
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            – D: 23
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              Text: 2025 Oct 23
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            – TitleFull: Molecular syndromology
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