Hasil Pencarian - Alexandra Keefe

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  1. 1
    P655: Performing long-read sequencing from dried blood spot cards

    P655: Performing long-read sequencing from dried blood spot cards oleh Sydney Ward, Joy Goffena, Sophie Storz, Miranda Galey, Alexandra Keefe, Cate Paschal, Anna Scott, Danny Miller

    Diterbitkan 2024-01-01
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  2. 2
    P014: Multiple cases of mosaic X-linked adrenoleukodystrophy in males identified through newborn screening

    P014: Multiple cases of mosaic X-linked adrenoleukodystrophy in males identified through newborn screening oleh Alexandra Keefe, Dana Jensen, Renee Bend, Michelle Morrow, Paul Kruszka, Lauren O'Grady, Florian Eichler, Angela Sun, James Bennett

    Diterbitkan 2024-01-01
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  3. 3
    P487: Increasing access to precise genetic diagnoses for inpatients at Seattle Children’s Hospital

    P487: Increasing access to precise genetic diagnoses for inpatients at Seattle Children’s Hospital oleh Abbey Scott, Lukas Kruidenier, Megan Sikes, Anita Beck, Katrina Dipple, Margaret Adam, Ian Glass, Jennifer Hayek, James Bennett, Ghayda Mirzaa, Alexandra Keefe, Tara Wenger

    Diterbitkan 2024-01-01
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  4. 4
    P193: Inpatient genetics consults for nondysmorphic children: Characteristics, testing patterns and diagnostic yield

    P193: Inpatient genetics consults for nondysmorphic children: Characteristics, testing patterns and diagnostic yield oleh Alexandra Keefe, Abbey Scott, Lukas Kruidenier, Megan Sikes, Anita Beck, Katrina Dipple, Jennifer Hayek, James Bennett, Ghayda Mirzaa, Margaret Adam, Ian Glass, Tara Wenger

    Diterbitkan 2024-01-01
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  5. 5
    Pask integrates hormonal signaling with histone modification via Wdr5 phosphorylation to drive myogenesis

    Pask integrates hormonal signaling with histone modification via Wdr5 phosphorylation to drive myogenesis oleh Chintan K Kikani, Xiaoying Wu, Litty Paul, Hana Sabic, Zuolian Shen, Arvind Shakya, Alexandra Keefe, Claudio Villanueva, Gabrielle Kardon, Barbara Graves, Dean Tantin, Jared Rutter

    Diterbitkan 2016-09-01
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  6. 6
    P414: SeqFirst: Parental perspectives on receiving results from neonatal rapid whole genome sequencing

    P414: SeqFirst: Parental perspectives on receiving results from neonatal rapid whole genome sequencing oleh Tara Wenger, Alexandra Keefe, Megan Sikes, Luke Kruidenier, Joon-Ho Yu, Kate McDuffie, Olivia Sommers, Heidi Gildersleeve, Abbey Scott, Chayna Davis, Paul Kruszka, Kati Buckingham, Jessica Chong, Kyle Retterer, Kirsty McWalter, Amy Snook, Jane Juusola, Deborah Copenheaver, David Veenstra, Danny Miller, Katrina Dipple, Michael Bamshad

    Diterbitkan 2023-01-01
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  7. 7
    P194: SeqFirst mitigates race-based disparities in access to a precise genetic diagnosis in hospitalized neonates

    P194: SeqFirst mitigates race-based disparities in access to a precise genetic diagnosis in hospitalized neonates oleh Tara Wenger, Alexandra Keefe, Lukas Kruidenier, Megan Sikes, Abbey Scott, Joon-Ho Yu, Kate MacDuffie, Kailyn Anderson, Olivia Sommers, Heidi Gildersleeve, Kati Buckingham, Jessica Chong, Katrina Dipple, David Veenstra, Dan Doherty, Daniel Miller, Deborah Copenheaver, Jane Juusola, Amy Snook, Chayna Davis, Kirsty McWalter, Paul Kruszka, Michael Bamshad

    Diterbitkan 2024-01-01
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  8. 8
    P208: SeqFirst: Impact of a precise genetic diagnosis on end-of-life decision making in the NICU*

    P208: SeqFirst: Impact of a precise genetic diagnosis on end-of-life decision making in the NICU* oleh Alexandra Keefe, Tara Wenger, Joon-Ho Yu, Megan Sikes, Luke Kruidenier, Abbey Scott, Kate McDuffie, Olivia Sommers, Heidi Gildersleeve, Chayna Davis, Paul Kruszka, Kati Buckingham, Jessica Chong, David Veenstra, Kyle Retterer, Kirsty McWalter, Amy Snook, Jane Juusola, Deborah Copenheaver, Danny Miller, Katrina Dipple, Kyle Brothers, Michael Bamshad

    Diterbitkan 2023-01-01
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  9. 9
    P214: SeqFirst DDi: Early whole genome sequencing improves access to early precise genetic diagnosis for children with developmental differences

    P214: SeqFirst DDi: Early whole genome sequencing improves access to early precise genetic diagnosis for children with developmental differences oleh Katrina Dipple, Daniel Doherty, Kailyn Anderson, Olivia Sommers, Tara Wenger, Kate MacDuffie, Alexandra Keefe, Abbey Scott, Lukas Kruidenier, Jamie Love-Nichols, Heidi Gildersleeve, Chayna Davis, Kati Buckingham, Jessica Chong, David Veenstra, Danny Miller, Deborah Copenheaver, Jane Juusola, Kyle Retterer, Kirsty McWalter, Paul Kruszka, Joon-Ho Yu, Michael Bamshad

    Diterbitkan 2024-01-01
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