Hasil Pencarian - Cate Paschal

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  1. 1
    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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  2. 2
    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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  3. 3
    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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  4. 4
    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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