Search Results - Raymond Caylor

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  1. 1

    P702: Impact of variant reclassification: Insights from Greenwood Genetic Center by Xuemei Shi, Fatima Abidi, Julie Jones, Raymond Caylor, Raymond Louie, Jennifer Lee, Michael Friez

    Published in Genetics in Medicine Open (2025-01-01)
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  2. 2

    P582: Exon-level copy number variations identified by whole genome sequencing in previously undiagnosed patients with rare hereditary diseases by Jiyong Wang, Raymond Caylor, Julie Jones, Jennifer Lee, Raymond Louie, Benjamin Hilton, Barbara DuPont, Kameryn Butler

    Published in Genetics in Medicine Open (2023-01-01)
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  3. 3

    P601: Clinical utility of MS-MLPA for the diagnosis of Prader-Willi/Angelman syndrome: The GGC experience by Xuemei Shi, Robin Fletcher, Jiyong Wang, Machenzie Lally, Sydney Posey, Michael Friez, Jennifer Lee, Raymond Caylor, Fatima Abidi

    Published in Genetics in Medicine Open (2024-01-01)
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  4. 4

    P569: Identification of a novel, deep-intronic alteration in KDM6A: How a multi-omics approach ended a 10+ year diagnostic odyssey* by Matthew Tedder, Jessica Cooley Coleman, Anna Childers, Jennifer Kerkhof, Raymond Louie, Jennifer Lee, Michael Friez, Bekim Sadikovic, David Everman, Richard Rogers, Raymond Caylor

    Published in Genetics in Medicine Open (2023-01-01)
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