P455: Milder symptom presentation of de novo NARS1 pathogenic variant: A case report by Teri Guo, Margaret Adam

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

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

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O43: Characterization of the prenatal renal phenotype associated with 17q12/HNF1B microdeletions by Courtney Verscaj, Frances Velez-Bartolomei, Ethan Bodle, Katie Chan, Michael Lyons, Willa Thorson, Wen-Hann Tan, John Graham, Angela Peron, Fabiola Quintero-Rivera, Elaine Zackai, Mary Ann Thomas, Cathy Stevens, Margaret Adam, Lynne Bird, Marilyn Jones, Dena Matalon

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