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First Prenatal Case of Genotypically and Phenotypically Overlapping Double Molecular Diagnosis of Van den Ende–Gupta and 22q11.2 Deletion Syndromes.

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Title: First Prenatal Case of Genotypically and Phenotypically Overlapping Double Molecular Diagnosis of Van den Ende–Gupta and 22q11.2 Deletion Syndromes.
Authors: Racine, Caroline1,2 (AUTHOR) caroline.racine@chu‐dijon.fr, Garde, Aurore1 (AUTHOR), Martz, Olivia3 (AUTHOR), Safraou, Hana2,4 (AUTHOR), Eluard, Vinciane3 (AUTHOR), Rousseau, Thierry3 (AUTHOR), Marle, Nathalie5 (AUTHOR), Harizay, Fara T.6 (AUTHOR), Martin, Laurent6 (AUTHOR), Maraval, Julien1 (AUTHOR), Bruel, Ange‐Line2,4 (AUTHOR), Philippe, Christophe2,4 (AUTHOR), Thauvin‐Robinet, Christel2,4 (AUTHOR), Faivre, Laurence1,2 (AUTHOR)
Source: Molecular Genetics & Genomic Medicine. Apr2025, Vol. 13 Issue 4, p1-8. 8p.
Database: Academic Search Ultimate
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  Data: <searchLink fieldCode="JN" term="%22Molecular+Genetics+%26+Genomic+Medicine%22">Molecular Genetics & Genomic Medicine</searchLink>. Apr2025, Vol. 13 Issue 4, p1-8. 8p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=184768406
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        Value: 10.1002/mgg3.70096
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        Text: English
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        PageCount: 8
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      – TitleFull: First Prenatal Case of Genotypically and Phenotypically Overlapping Double Molecular Diagnosis of Van den Ende–Gupta and 22q11.2 Deletion Syndromes.
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              Text: Apr2025
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              Y: 2025
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