Hasil Pencarian - Danny Miller

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  1. 1
    P824: GREGoR: Increasing rare disease diagnosis using emerging technologies and data sharing

    P824: GREGoR: Increasing rare disease diagnosis using emerging technologies and data sharing oleh Danny Miller

    Diterbitkan 2024-01-01
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  2. 2
    Narcisismo e liderança: uma perspectiva de relações de objetos

    Narcisismo e liderança: uma perspectiva de relações de objetos oleh Manfred F. R. Kets de Vries, Danny Miller

    Diterbitkan 1990-07-01
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  3. 3
    The Routledge Handbook of Sustainable Real Estate

    The Routledge Handbook of Sustainable Real Estate oleh Sara Wilkinson, Tim Dixon, Danny Norm, Danny Miller, Sarah Sayce

    Diterbitkan 2018-01-01
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  4. 4
    P246: Five-year retrospective case series of genetic findings in patients with planned surgical interventions for cardiac left-right patterning differences

    P246: Five-year retrospective case series of genetic findings in patients with planned surgical interventions for cardiac left-right patterning differences oleh Jonathan Marquez, Lauren Carlozzi, Danny Miller, Matthew Files, BreAnna Kinghorn, Eyal Sagiv

    Diterbitkan 2023-01-01
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  5. 5
    O33: Concordance of long-read genome sequencing with methylation calling with clinical testing for individuals with Prader-Willi or Angelman Syndrome*

    O33: Concordance of long-read genome sequencing with methylation calling with clinical testing for individuals with Prader-Willi or Angelman Syndrome* oleh Cate Paschal, Anita Beck, Madelyn Gillentine, Jaya Narayanan, Paxton Reed, Miranda Galey, Danny Miller

    Diterbitkan 2023-01-01
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  6. 6
    P630: Multi-modal testing, including long-read sequencing, to elucidate an unsolved case of dyskeratosis congenita

    P630: Multi-modal testing, including long-read sequencing, to elucidate an unsolved case of dyskeratosis congenita oleh Ankita Jhuraney, Sarah Paolucci, Sophia Gibson, Nikhita Damaraju, Danny Miller, Jennifer Hayek, Bri Dingmann, Jillian Buchan

    Diterbitkan 2024-01-01
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  7. 7
    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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  8. 8
    P364: Mosaic copy gain of 16p with supernumerary chromosome formation: An emerging phenotype

    P364: Mosaic copy gain of 16p with supernumerary chromosome formation: An emerging phenotype oleh Arthur Lenahan, Ian Glass, Andrew Stergachis, Cate Paschal, Elizabeth Blue, Aimee Allworth, Ingrid Cristian, Danny Miller, Jennifer Morrison

    Diterbitkan 2024-01-01
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  9. 9
    P672: Long-read sequencing reveals a novel pathogenic variant in IKBKG with associated skewed X-inactivation in affected females

    P672: Long-read sequencing reveals a novel pathogenic variant in IKBKG with associated skewed X-inactivation in affected females oleh Danny Miller, Camille Dash, David Miller, Miranda Galey, Jasmine Lin, Jill A. Madden, Alan Beggs, Pankaj Agrawal, Casie Genetti, Monica Wojcik

    Diterbitkan 2023-01-01
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  10. 10
    P438: Clinical RNA sequencing to clarify variants of uncertain significance and identify missing variants

    P438: Clinical RNA sequencing to clarify variants of uncertain significance and identify missing variants oleh Jennifer Cech, Danny Miller, Cate Paschal, Bri Dingmann, Anna Scott, Jenny Thies, Maria Mills, J. Lawrence Merritt, II, Ghayda Mirzaa, James Bennett, Ian Glass, Darci Sternen, Heather Mefford

    Diterbitkan 2023-01-01
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  11. 11
    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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  12. 12
    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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  13. 13
    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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