Works matching IS 00034800 AND DT 2024 AND VI 88 AND IP 2


Results: 7
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    Low‐pass whole genome sequencing is a reliable and cost‐effective approach for copy number variant analysis in the clinical setting.

    Published in:
    Annals of Human Genetics, 2024, v. 88, n. 2, p. 113, doi. 10.1111/ahg.12532
    By:
    • Mazzonetto, Patricia C.;
    • Villela, Darine;
    • da Costa, Silvia Souza;
    • Krepischi, Ana C. V.;
    • Milanezi, Fernanda;
    • Migliavacca, Michele P.;
    • Pierry, Paulo M.;
    • Bonaldi, Adriano;
    • Almeida, Luiz Gustavo D.;
    • De Souza, Camila Alves;
    • Kroll, José Eduardo;
    • Paula, Marcelo G.;
    • Guarischi‐Sousa, Rodrigo;
    • Scapulatempo‐Neto, Cristovam;
    • Rosenberg, Carla
    Publication type:
    Article
    3

    Issue Information.

    Published in:
    Annals of Human Genetics, 2024, v. 88, n. 2, p. 1, doi. 10.1111/ahg.12513
    Publication type:
    Article
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