Showing 1 - 4 results of 4 for search 'Cate Paschal', query time: 0.02s Refine Results
  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* by Cate Paschal, Anita Beck, Madelyn Gillentine, Jaya Narayanan, Paxton Reed, Miranda Galey, Danny Miller

    Published 2023-01-01
    Get full text
    Article
  2. 2
    P655: Performing long-read sequencing from dried blood spot cards

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

    Published 2024-01-01
    Get full text
    Article
  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 by Arthur Lenahan, Ian Glass, Andrew Stergachis, Cate Paschal, Elizabeth Blue, Aimee Allworth, Ingrid Cristian, Danny Miller, Jennifer Morrison

    Published 2024-01-01
    Get full text
    Article
  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 by 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

    Published 2023-01-01
    Get full text
    Article

Search Tools: