Hasil Pencarian - Hutton Kearney

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  1. 1
    P815: Prenatal diagnosis of tetrasomy 21: Case reports

    P815: Prenatal diagnosis of tetrasomy 21: Case reports oleh Kyna Byerly, Kristen Nye, Hutton Kearney, Nicole Hoppman

    Diterbitkan 2024-01-01
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  2. 2
    P473: Potential clinical significance of microdeletions involving both MYH6 and MYH7

    P473: Potential clinical significance of microdeletions involving both MYH6 and MYH7 oleh McKinsey Goodenberger, Nicole Hoppman, Hutton Kearney, Kristen Rasmussen

    Diterbitkan 2023-01-01
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  3. 3
    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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  4. 4
    P672: Commercial cystic fibrosis carrier screening tests and coverage of the ACMG 100 recommended variants

    P672: Commercial cystic fibrosis carrier screening tests and coverage of the ACMG 100 recommended variants oleh Timothy Tidwell, Anthony Gregg, Wayne Grody, Michael Guo, Hutton Kearney, Kristin Monaghan, Jennifer Taylor, Cinthya Zepeda Mendoza, Catherine Ziats, Joshua Deignan, Karen Raraigh

    Diterbitkan 2024-01-01
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  5. 5
    P589: Improved efficiency of G-band chromosome analysis via deep neural network workflow

    P589: Improved efficiency of G-band chromosome analysis via deep neural network workflow oleh Xinjie Xu, Derek Slagter, Todd VanDeWalker, Erin Theobald, Tina Brown, Daniel Hoppe, Sheryl Castro, Joel Denney, Jennifer Gardner, Christopher Stahl, Hutton Kearney, Jansen Seheult, Carley Ann Suarez, Harshawardhan Banda

    Diterbitkan 2023-01-01
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