Exome Sequencing for Prenatal Diagnosis in Nonimmune Hydrops Fetalis von Sparks, Teresa N, Lianoglou, Billie R, Adami, Rebecca R, Pluym, Ilina D, Holliman, Kerry, Duffy, Jennifer, Downum, Sarah L, Patel, Sachi, Faubel, Amanda, Boe, Nina M, Field, Nancy T, Murphy, Aisling, Laurent, Louise C, Jolley, Jennifer, Uy, Cherry, Slavotinek, Anne M, Devine, Patrick, Hodoglugil, Ugur, Van Ziffle, Jessica, Sanders, Stephan J, MacKenzie, Tippi C, Norton, Mary E

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Exome sequencing vs targeted gene panels for the evaluation of nonimmune hydrops fetalis von Norton, Mary E., Ziffle, Jessica Van, Lianoglou, Billie R., Hodoglugil, Ugur, Devine, W. Patrick, Sparks, Teresa N.

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In Utero Enzyme-Replacement Therapy for Infantile-Onset Pompe’s Disease von Cohen, Jennifer L., Chakraborty, Pranesh, Fung-Kee-Fung, Karen, Schwab, Marisa E., Bali, Deeksha, Young, Sarah P., Gelb, Michael H., Khaledi, Hamid, DiBattista, Alicia, Smallshaw, Stacey, Moretti, Felipe, Wong, Derek, Lacroix, Catherine, El Demellawy, Dina, Strickland, Kyle C., Lougheed, Jane, Moon-Grady, Anita, Lianoglou, Billie R., Harmatz, Paul, Kishnani, Priya S., MacKenzie, Tippi C.

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Access to prenatal exome sequencing for fetal malformations: A qualitative landscape analysis in the US von Sahin‐Hodoglugil, Nuriye N., Lianoglou, Billie R., Ackerman, Sara, Sparks, Teresa N., Norton, Mary E.

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Intrauterine enzyme replacement therapies for lysosomal storage disorders: Current developments and promising future prospects von Herzeg, Akos, Borges, Beltran, Lianoglou, Billie R., Gonzalez‐Velez, Juan, Canepa, Emma, Munar, Dane, Young, Sarah P., Bali, Deeksha, Gelb, Michel H., Chakraborty, Pranesh, Kishnani, Priya S., Harmatz, Paul, Cohen, Jennifer L., MacKenzie, Tippi C.

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Nonimmune hydrops fetalis: identifying the underlying genetic etiology von Sparks, Teresa N., Thao, Kao, Lianoglou, Billie R., Boe, Nina M., Bruce, Kari G., Datkhaeva, Ilina, Field, Nancy T., Fratto, Victoria M., Jolley, Jennifer, Laurent, Louise C., Mardy, Anne H., Murphy, Aisling M., Ngan, Emily, Rangwala, Naseem, Rottkamp, Catherine A. M., Wilson, Lisa, Wu, Erica, Uy, Cherry C., Valdez Lopez, Priscila, Norton, Mary E.

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Preference for secondary findings in prenatal and pediatric exome sequencing von Swanson, Kate, Sparks, Teresa N., Lianoglou, Billie R., Chen, Flavia, Downum, Sarah, Patel, Sachi, Rego, Shannon, Yip, Tiffany, Ziffle, Jessica, Koenig, Barbara A., Slavotinek, Anne M., Norton, Mary E.

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The utility of pathologic examination and comprehensive phenotyping for accurate diagnosis with perinatal exome sequencing von Swanson, Kate, Norton, Mary E., Lianoglou, Billie R., Jelin, Angie C., Hodoglugil, Ugur, Ziffle, Jessica, Devine, Patrick, Sparks, Teresa N.

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Trust in prenatal exome sequencing for expectant families facing unexplained fetal anomalies von Rothschild, Harriet T., Lianoglou, Billie R., Sahin Hodoglugil, Nuriye N., Tick, Katie, Brown, Julia E. H., Sparks, Teresa N.

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Exome sequencing of fetuses with congenital diaphragmatic hernia supports a causal role for NR2F2, PTPN11, and WT1 variants von Schwab, Marisa E., Dong, Shan, Lianoglou, Billie R., Aguilar Lucero, Alessandra F., Schwartz, Grace B., Norton, Mary E., MacKenzie, Tippi C., Sanders, Stephan J.

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"Let's Just Wait Until She's Born": Temporal Factors That Shape Decision-Making for Prenatal Genomic Sequencing Amongst Families Underrepresented in Genomic Research von Brown, Julia E H, Zamora, Astrid N, Outram, Simon, Sparks, Teresa N, Lianoglou, Billie R, Norstad, Matthew, Sahin Hodoglugil, Nuriye N, Norton, Mary E, Ackerman, Sara L

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Fetal therapies and trials for lysosomal storage diseases: a survey of attitudes of parents and patients von Schwab, Marisa E, Brown, Julia E H, Lianoglou, Billie, Jin, Chengshi, Conroy, Patricia C, Gallagher, Renata C, Harmatz, Paul, MacKenzie, Tippi C

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P027: Analysis of glycosaminoglyans in biological fluids reveals diverging trends in heparan sulfate, dermatan sulfate and chondroitine sulfate concentrations with age von Menkovic, Iskren, Beasley, James, Zhang, Haoyue, Lianoglou, Billie, Yu, Jingwei, Stiles, Ashlee, Harmatz, Paul, Young, Sarah

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Patient understanding of prenatal exome sequencing von Swanson, Kate, Norton, Mary E, Ackerman, Sara L, Lianoglou, Billie R, Sahin-Hodoglugil, Nuriye N, Sparks, Teresa N

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O41: Genes associated with disease in fetuses compared to children: Exome sequencing in a large pediatric and prenatal cohort von Sparks, Teresa, Lianoglou, Billie, Sahin-Holodlugil, Nuriye, Kvale, Mark, Van Ziffle, Jessica, Devine, W. Patrick, Hodoglugil, Ugur, Martin, Pierre-Marie, Koenig, Barbara, Kwok, Pui-Yan, Ackerman, Sara, Slavotinek, Anne, Risch, Neil, Norton, Mary

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Consensus statement for the perinatal management of patients with α thalassemia major von MacKenzie, Tippi C., Amid, Ali, Angastiniotis, Michael, Butler, Craig, Gilbert, Sandra, Gonzalez, Juan, Keller, Roberta L., Kharbanda, Sandhya, Kirby-Allen, Melanie, Koenig, Barbara A., Kyono, Wade, Lal, Ashutosh, Lianoglou, Billie R., Norton, Mary E., Ogasawara, Keith K., Panchalee, Tachjaree, Rosner, Mara, Schwab, Marisa, Thompson, Alexis, Waye, John S., Vichinsky, Elliott

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The impact of in utero transfusions on perinatal outcomes in patients with alpha thalassemia major: the UCSF registry von Schwab, Marisa E., Lianoglou, Billie R., Gano, Dawn, Gonzalez Velez, Juan, Allen, Isabel E., Arvon, Regina, Baschat, Ahmet, Bianchi, Diana W., Bitanga, Melissa, Bourguignon, Anne, Brown, Richard N., Chen, Bruce, Chien, May, Davis-Nelson, Shareece, de Laat, Monique W. M., Ekwattanakit, Supachai, Gollin, Yvonne, Hirata, Greigh, Jelin, Angie, Jolley, Jennifer, Meyer, Paul, Miller, Jena, Norton, Mary E., Ogasawara, Keith K., Panchalee, Tachjaree, Schindewolf, Erica, Shaw, Steven W., Stumbaugh, Tammy, Thompson, Alexis A., Towner, Dena, Tsai, Pai-Jong Stacy, Viprakasit, Vip, Volanakis, Emmanuel, Zhang, Li, Vichinsky, Elliott, MacKenzie, Tippi C.

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Genomic Sequencing Results Disclosure in Diverse and Medically Underserved Populations: Themes, Challenges, and Strategies from the CSER Consortium von Suckiel, Sabrina A., O'Daniel, Julianne M., Donohue, Katherine E., Gallagher, Katie M., Gilmore, Marian J., Hendon, Laura G., Joseph, Galen, Lianoglou, Billie R., Mathews, Jennifer M., Norton, Mary E., Odgis, Jacqueline A., Poss, Alexis F., Rego, Shannon, Scollon, Sarah, Yip, Tiffany, Amendola, Laura M.

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O40: Clinical utility of prenatal exome sequencing in a diverse cohort von Norton, Mary, Lianoglou, Billie, Shear, Matthew, Ackerman, Sara, Sahin-Holodlugil, Nuriye, Kvale, Mark, Van Ziffle, Jessica, Devine, W. Patrick, Hodoglugil, Ugur, Martin, Pierre-Marie, Koenig, Barbara, Risch, Neil, Kwok, Pui-Yan, Slavotinek, Anne, Sparks, Teresa

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234 Expanded carrier screening for genetic conditions with clinical trials in-utero therapy von Lianoglou, Billie R., Souter, Vivienne, Prigmore, Brittany, Repass, Elizabeth, Wang, Yang, MacKenzie, Tippi C.

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