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

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

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P214: SeqFirst DDi: Early whole genome sequencing improves access to early precise genetic diagnosis for children with developmental differences von Dipple, Katrina, Doherty, Daniel, Anderson, Kailyn, Sommers, Olivia, Wenger, Tara, MacDuffie, Kate, Keefe, Alexandra, Scott, Abbey, Kruidenier, Lukas, Love-Nichols, Jamie, Gildersleeve, Heidi, Davis, Chayna, Buckingham, Kati, Chong, Jessica, Veenstra, David, Miller, Danny, Copenheaver, Deborah, Juusola, Jane, Retterer, Kyle, McWalter, Kirsty, Kruszka, Paul, Yu, Joon-Ho, Bamshad, Michael

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P194: SeqFirst mitigates race-based disparities in access to a precise genetic diagnosis in hospitalized neonates von Wenger, Tara, Keefe, Alexandra, Kruidenier, Lukas, Sikes, Megan, Scott, Abbey, Yu, Joon-Ho, MacDuffie, Kate, Anderson, Kailyn, Sommers, Olivia, Gildersleeve, Heidi, Buckingham, Kati, Chong, Jessica, Dipple, Katrina, Veenstra, David, Doherty, Dan, Miller, Daniel, Copenheaver, Deborah, Juusola, Jane, Snook, Amy, Davis, Chayna, McWalter, Kirsty, Kruszka, Paul, Bamshad, Michael

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