Maternal uniparental disomy of chromosome 20: a novel imprinting disorder of growth failure von Mulchandani, Surabhi, Bhoj, Elizabeth J., Luo, Minjie, Powell-Hamilton, Nina, Jenny, Kim, Gripp, Karen W., Elbracht, Miriam, Eggermann, Thomas, Turner, Claire L.S., Temple, I. Karen, Mackay, Deborah J.G., Dubbs, Holly, Stevenson, David A., Slattery, Leah, Zackai, Elaine H., Spinner, Nancy B., Krantz, Ian D., Conlin, Laura K.

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Facilitating Test Status Information Communication in the Time of COVID-19 von Master, Stephen R., Neide, Brandy, Kollu, Sunaina, Mulchandani, Surabhi, Harris, Rebecca M., Obstfeld, Amrom E.

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P532: Development, implementation, and preliminary results of rapid targeted genomic analysis in the newborn period von Bedoukian, Emma, Reichert, Sara, DeChene, Elizabeth, Heck, Alexandra, Hershey, Jennifer, McManus, Morgan, Marchese, Michelle, Mulchandani, Surabhi, Reynoso Santos, Francis Jeshira, Wild, K. Taylor, Wood, Kathleen, Conlin, Laura, Dulik, Matthew, Rajagopalan, Ramakrishnan, Spinner, Nancy, Krantz, Ian

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Interstitial microduplication of Xp22.31: Causative of intellectual disability or benign copy number variant? von Li, Feng, Shen, Yiping, Köhler, Udo, Sharkey, Freddie H, Menon, Deepa, Coulleaux, Laurence, Malan, Valérie, Rio, Marlène, McMullan, Dominic J, Cox, H, Fagan, Kerry A, Gaunt, Lorraine, Metcalfe, Kay, Heinrich, Uwe, Hislop, Gordon, Maye, Una, Sutcliffe, Maxine, Wu, Bai-Lin, Thiel, Brian D, Mulchandani, Surabhi, Conlin, Laura K, Spinner, Nancy B, Murphy, Kathleen M, Batista, Denise A.S

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Parents’ Perceptions of the Usefulness of Chromosomal Microarray Analysis for Children with Autism Spectrum Disorders von Reiff, Marian, Giarelli, Ellen, Bernhardt, Barbara A., Easley, Ebony, Spinner, Nancy B., Sankar, Pamela L., Mulchandani, Surabhi

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“Set in Stone” or “Ray of Hope”: Parents’ Beliefs About Cause and Prognosis After Genomic Testing of Children Diagnosed with ASD von Reiff, Marian, Bugos, Eva, Giarelli, Ellen, Bernhardt, Barbara A., Spinner, Nancy B., Sankar, Pamela L., Mulchandani, Surabhi

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“What does it mean?”: Uncertainties in understanding results of chromosomal microarray testing von Reiff, Marian, Bernhardt, Barbara A., Mulchandani, Surabhi, Soucier, Danielle, Cornell, Diana, Pyeritz, Reed E., Spinner, Nancy B.

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Physicians' perspectives on the uncertainties and implications of chromosomal microarray testing of children and families von Reiff, M, Ross, K, Mulchandani, S, Propert, KJ, Pyeritz, RE, Spinner, NB, Bernhardt, BA

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Use of a Dynamic Genetic Testing Approach for Childhood-Onset Epilepsy von Balciuniene, Jorune, DeChene, Elizabeth T, Akgumus, Gozde, Romasko, Edward J, Cao, Kajia, Dubbs, Holly A, Mulchandani, Surabhi, Spinner, Nancy B, Conlin, Laura K, Marsh, Eric D, Goldberg, Ethan, Helbig, Ingo, Sarmady, Mahdi, Abou Tayoun, Ahmad

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Clinical features of three girls with mosaic genome-wide paternal uniparental isodisomy von Kalish, Jennifer M., Conlin, Laura K., Bhatti, Tricia R., Dubbs, Holly A., Harris, Mary Catherine, Izumi, Kosuke, Mostoufi-Moab, Sogol, Mulchandani, Surabhi, Saitta, Sulagna, States, Lisa J., Swarr, Daniel T., Wilkens, Alisha B., Zackai, Elaine H., Zelley, Kristin, Bartolomei, Marisa S., Nichols, Kim E., Palladino, Andrew A., Spinner, Nancy B., Deardorff, Matthew A.

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CMIP haploinsufficiency in two patients with autism spectrum disorder and co‐occurring gastrointestinal issues von Luo, Minjie, Fan, Jinbo, Wenger, Tara L., Harr, Margaret H., Racobaldo, Melissa, Mulchandani, Surabhi, Dubbs, Holly, Zackai, Elaine H., Spinner, Nancy B., Conlin, Laura K.

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A Qualitative Study of Healthcare Providers’ Perspectives on the Implications of Genome-Wide Testing in Pediatric Clinical Practice von Reiff, Marian, Mueller, Rebecca, Mulchandani, Surabhi, Spinner, Nancy B., Pyeritz, Reed E., Bernhardt, Barbara A.

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Detection of mutually exclusive mosaicism in a girl with genotype-phenotype discrepancies von Luo, Minjie, Mulchandani, Surabhi, Dubbs, Holly A., Swarr, Daniel, Pyle, Louise, Zackai, Elaine H., Spinner, Nancy B., Conlin, Laura K.

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Subtelomeric deletion of chromosome 10p15.3: Clinical findings and molecular cytogenetic characterization von DeScipio, Cheryl, Conlin, Laura, Rosenfeld, Jill, Tepperberg, James, Pasion, Romela, Patel, Ankita, McDonald, Marie T., Aradhya, Swaroop, Ho, Darlene, Goldstein, Jennifer, McGuire, Marianne, Mulchandani, Surabhi, Medne, Livija, Rupps, Rosemarie, Serrano, Alvaro H., Thorland, Erik C., Tsai, Anne C.-H., Hilhorst-Hofstee, Yvonne, Ruivenkamp, Claudia A.L., Van Esch, Hilde, Addor, Marie-Claude, Martinet, Danielle, Mason, Thornton B.A., Clark, Dinah, Spinner, Nancy B., Krantz, Ian D.

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Assessing Copy Number Variants Involving ACMGG Secondary Finding Genes Identified by Routine Chromosomal SNP Array in a Clinical Pediatric Population von Fan, Jinbo, Mulchandani, Surabhi, Dulik, Matthew, Chen, Jinyun, Gleason, Adam, Jayaraman, Pushkala, Sarmady, Mahdi, Zackai, Elaine, Luo, Minjie, Spinner, Nancy, Conlin, Laura

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4 - Assessing Copy Number Variants Involving ACMGG Secondary Finding Genes Identified by Routine Chromosomal SNP Array in a Clinical Pediatric Population von Fan, Jinbo, Mulchandani, Surabhi, Dulik, Matthew, Chen, Jinyun, Gleason, Adam, Jayaraman, Pushkala, Sarmady, Mahdi, Zackai, Elaine, Luo, Minjie, Spinner, Nancy, Conlin, Laura

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Mosaic maternal uniparental disomy of chromosome 15 in Prader–Willi syndrome: Utility of genome‐wide SNP array von Izumi, Kosuke, Santani, Avni B., Deardorff, Matthew A., Feret, Holly A., Tischler, Tanya, Thiel, Brian D., Mulchandani, Surabhi, Stolle, Catherine A., Spinner, Nancy B., Zackai, Elaine H., Conlin, Laura K.

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Bilateral Pheochromocytomas, Hemihyperplasia, and Subtle Somatic Mosaicism: The Importance of Detecting Low-Level Uniparental Disomy von Kalish, Jennifer M., Conlin, Laura K., Mostoufi-Moab, Sogol, Wilkens, Alisha B., Mulchandani, Surabhi, Zelley, Kristin, Kowalski, Megan, Bhatti, Tricia R., Russo, Pierre, Mattei, Peter, Mackenzie, William G., LiVolsi, Virginia, Nichols, Kim E., Biegel, Jaclyn A., Spinner, Nancy B., Deardorff, Matthew A.

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Genomic variation: what does it mean? von Reiff, Marian, Bernhardt, Barbara A, Mulchandani, Surabhi

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Mosaic trisomy 17: Variable clinical and cytogenetic presentation von Daber, Robert, Chapman, Kimberly A., Ruchelli, Eduardo, Kasperski, Stefanie, Mulchandani, Surabhi, Thiel, Brian D., Hakonarson, Hakon, Zackai, Elaine H., Conlin, Laura K., Spinner, Nancy B.

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