Hasil Pencarian - Cassandra Runke

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  1. 1
    P707: Additional evidence supporting and expanding the phenotype associated with MED12L loss-of-function variants

    P707: Additional evidence supporting and expanding the phenotype associated with MED12L loss-of-function variants oleh Kristen Rasmussen, Cassandra Runke, Sarah Barnett, Hutton Kearney, Erik Thorland

    Diterbitkan 2024-01-01
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  2. 2
    P536: 2q11.2 recurrent CNVs including TMEM127: A collaborative multi-center study to expand knowledge of neurodevelopmental phenotypes and pheochromocytoma/paraganglioma syndrome predisposition

    P536: 2q11.2 recurrent CNVs including TMEM127: A collaborative multi-center study to expand knowledge of neurodevelopmental phenotypes and pheochromocytoma/paraganglioma syndrome p... oleh Lucilla Pizzo, Zoe Lewis, Lauren Walsh, Cassandra Runke, Margit Nõukas, Katrin Männik, Neeme Tõnisson, Erik Thorland, Christa Martin, Katie Rudd, Erica Andersen

    Diterbitkan 2023-01-01
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  3. 3
    P485: Evaluating novel dosage sensitivity predictors for inclusion in the classification of recurrent copy number variants

    P485: Evaluating novel dosage sensitivity predictors for inclusion in the classification of recurrent copy number variants oleh John Herriges, Cassandra Runke, Zoe Lewis, Lucilla Pizzo, Bradley Coe, Laura Conlin, Benjamin Hilton, Brynn Levy, Andrea Vaags, Shulin Zhang, Christa Martin, Erica Andersen

    Diterbitkan 2023-01-01
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