P824: GREGoR: Increasing rare disease diagnosis using emerging technologies and data sharing by Danny Miller

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Narcisismo e liderança: uma perspectiva de relações de objetos by Manfred F. R. Kets de Vries, Danny Miller

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The Routledge Handbook of Sustainable Real Estate by Sara Wilkinson, Tim Dixon, Danny Norm, Danny Miller, Sarah Sayce

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P246: Five-year retrospective case series of genetic findings in patients with planned surgical interventions for cardiac left-right patterning differences by Jonathan Marquez, Lauren Carlozzi, Danny Miller, Matthew Files, BreAnna Kinghorn, Eyal Sagiv

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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

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P630: Multi-modal testing, including long-read sequencing, to elucidate an unsolved case of dyskeratosis congenita by Ankita Jhuraney, Sarah Paolucci, Sophia Gibson, Nikhita Damaraju, Danny Miller, Jennifer Hayek, Bri Dingmann, Jillian Buchan

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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

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Effects of manual osteopathic interventions on psychometric and psychophysiological indicators of anxiety, depression and stress in adults: a systematic review and meta-analysis of... by Darren J Edwards, Jerry Draper-Rodi, Danny Miller, Josh Hope-Bell, Andrew MacMillan, Tom C Gordon

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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

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P672: Long-read sequencing reveals a novel pathogenic variant in IKBKG with associated skewed X-inactivation in affected females by Danny Miller, Camille Dash, David Miller, Miranda Galey, Jasmine Lin, Jill A. Madden, Alan Beggs, Pankaj Agrawal, Casie Genetti, Monica Wojcik

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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

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P414: SeqFirst: Parental perspectives on receiving results from neonatal rapid whole genome sequencing by Tara Wenger, Alexandra Keefe, Megan Sikes, Luke Kruidenier, Joon-Ho Yu, Kate McDuffie, Olivia Sommers, Heidi Gildersleeve, Abbey Scott, Chayna Davis, Paul Kruszka, Kati Buckingham, Jessica Chong, Kyle Retterer, Kirsty McWalter, Amy Snook, Jane Juusola, Deborah Copenheaver, David Veenstra, Danny Miller, Katrina Dipple, Michael Bamshad

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P208: SeqFirst: Impact of a precise genetic diagnosis on end-of-life decision making in the NICU* by Alexandra Keefe, Tara Wenger, Joon-Ho Yu, Megan Sikes, Luke Kruidenier, Abbey Scott, Kate McDuffie, Olivia Sommers, Heidi Gildersleeve, Chayna Davis, Paul Kruszka, Kati Buckingham, Jessica Chong, David Veenstra, Kyle Retterer, Kirsty McWalter, Amy Snook, Jane Juusola, Deborah Copenheaver, Danny Miller, Katrina Dipple, Kyle Brothers, Michael Bamshad

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

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