Works matching DE "DUAL diagnosis"


Results: 1412
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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.

    Published in:
    Molecular Genetics & Genomic Medicine, 2025, v. 13, n. 4, p. 1, doi. 10.1002/mgg3.70096
    By:
    • Racine, Caroline;
    • Garde, Aurore;
    • Martz, Olivia;
    • Safraou, Hana;
    • Eluard, Vinciane;
    • Rousseau, Thierry;
    • Marle, Nathalie;
    • Harizay, Fara T.;
    • Martin, Laurent;
    • Maraval, Julien;
    • Bruel, Ange‐Line;
    • Philippe, Christophe;
    • Thauvin‐Robinet, Christel;
    • Faivre, Laurence
    Publication type:
    Article
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