Exploring experiences and expectations of prenatal health care and genetic counseling/testing in immigrant Latinas von Garza, Georgiann, Hodges‐Delgado, Priscila, Hoskovec, Jennifer, Palos, Guadalupe, Wagner, Chelsea, Zacharias, Nikolaos, Noblin, Sarah J.

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Patients with unexplained mismatch repair deficiency are interested in updated genetic testing von Omark, Jessica, Vilar, Eduardo, You, Y Nancy, Dunnington, Leslie, Noblin, Sarah, Stevens, Blair, Mork, Maureen

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Introduction of cell‐free DNA screening is associated with changes in prenatal genetic counseling indications von Stevens, Blair K., Noblin, Sarah J., Chen, Han‐Yang, Czerwinski, Jennifer, Friel, Lara A., Wagner, Chelsea

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Survival of Texas infants born with trisomies 21, 18, and 13 von Vendola, Catherine, Canfield, Mark, Daiger, Stephen P., Gambello, Michael, Hashmi, S. Shahrukh, King, Terri, Noblin, Sarah J., Waller, D. Kim, Hecht, Jacqueline T.

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First Neonatal Demise with Travel-Associated Zika Virus Infection in the United States of America von Zacharias, Nikolaos, Whitty, Janice, Noblin, Sarah, Tsakiri, Sophia, Garcia, Jose, Covinsky, Michael, Bhattacharjee, Meenakshi, Saulino, David, Tatevian, Nina, Blackwell, Sean

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Indications for genetic referral: a guide for healthcare providers von Pletcher, Beth A, Toriello, Helga V, Noblin, Sarah J, Seaver, Laurie H, Driscoll, Deborah A, Bennett, Robin L, Gross, Susan J

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Perceptions of Latinas on the Traditional Prenatal Genetic Counseling Model von Thompson, Stephanie, Noblin, Sarah Jane, Lemons, Jennifer, Peterson, Susan K., Carreno, Carlos, Harbison, Andrea

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The psychosocial effects of the Li-Fraumeni Education and Early Detection (LEAD) program on individuals with Li-Fraumeni syndrome von Ross, Jessica, Bojadzieva, Jasmina, Peterson, Susan, Noblin, Sarah Jane, Yzquierdo, Rebecca, Askins, Martha, Strong, Louise

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Somatic mismatch repair testing in evaluation of Lynch syndrome: The gap between preferred and current practices von Williams, Danielle, Vilar, Eduardo, Shakrukh Hashmi, S., Choates, Meagan, Noblin, Sarah, Mork, Maureen

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eP303: A tale of two tests: A PGT-M and expanded carrier screening clinical experience study von Wolfe, Ashton, Maisenbacher, Melissa, Palsuledesai, Charuta, Pastrick, Meredith, Noblin, Sarah, Adsit, Jessica, Hajjar, Mark, Ratousi, Dalar, Meyer, Liza, Wood, McKenzie, Fong, Megan, Yavari, Maygol, McNeill, Gabriel, Bai, Yan, Howard, Katherine

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Knowledge and Self-Esteem of Individuals with Neurofibromatosis Type 1 (NF1) von Rosnau, Kayla, Hashmi, S. Shahrukh, Northrup, Hope, Slopis, John, Noblin, Sarah, Ashfaq, Myla

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The utilization of prenatal microarray: A survey of current genetic counseling practices and barriers von Durham, Leslie, Papanna, Ramesha, Stevens, Blair, Noblin, Sarah, Rodriguez‐Buritica, David, Hashmi, S. Shahrukh, Krstic, Nevena

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Genetic Testing Practices of Genetic Counselors, Geneticists, and Pediatric Neurologists With Regard to Childhood-Onset Neurogenetic Conditions von Wofford, Sara, Noblin, Sarah, Davis, Jessica M, Farach, Laura S, Hashmi, S Shahrukh, Mancias, Pedro, Wagner, Victoria F

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Undergraduate Student Perceptions and Awareness of Genetic Counseling von Gerard, Amanda, Noblin, Sarah, Hashmi, S. Shahrukh, Bean, Andrew J., Bergstrom, Katie, Hurst, Christina B., Mattox, William, Stevens, Blair

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Attitudes Towards Prenatal Genetic Counseling, Prenatal Genetic Testing, and Termination of Pregnancy among Southeast and East Asian Women in the United States von Tsai, Ginger J., Cameron, Carrie A., Czerwinski, Jennifer L., Mendez-Figueroa, Hector, Peterson, Susan K., Noblin, Sarah Jane

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2013 Review and Update of the Genetic Counseling Practice Based Competencies by a Task Force of the Accreditation Council for Genetic Counseling von Doyle, Debra Lochner, Awwad, Rawan I., Austin, Jehannine C., Baty, Bonnie J., Bergner, Amanda L., Brewster, Stephanie J., Erby, Lori A. H., Franklin, Cathi Rubin, Greb, Anne E., Grubs, Robin E., Hooker, Gillian W., Noblin, Sarah Jane, Ormond, Kelly E., Palmer, Christina G., Petty, Elizabeth M., Singletary, Claire N., Thomas, Matthew J., Toriello, Helga, Walton, Carol S., Uhlmann, Wendy R.

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A patient with isochromosome 18q, radial‐thumb aplasia, thrombocytopenia, and an unbalanced 10;18 chromosome translocation von Sahoo, Trilochan, Naeem, Rizwan, Pham, Kim, Chheng, Sou, Noblin, Sarah T., Bacino, Carlos A., Gambello, Michael J.

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Is it all Lynch syndrome?: An assessment of family history in individuals with mismatch repair–deficient tumors von Dempsey, Katherine M., Broaddus, Russell, You, Y. Nancy, Noblin, Sarah Jane, Mork, Maureen, Fellman, Bryan, Urbauer, Diana, Daniels, Molly, Lu, Karen

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Exploring the Role of Religiosity and Spirituality in Amniocentesis Decision-Making Among Latinas von Seth, Sarah Guerra, Goka, Thomas, Harbison, Andrea, Hollier, Lisa, Peterson, Susan, Ramondetta, Lois, Noblin, Sarah Jane

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National Society of Genetic Counselors Code of Ethics: Explication of 2017 Revisions von Senter, Leigha, Bennett, Robin L., Madeo, Anne C., Noblin, Sarah, Ormond, Kelly E., Schneider, Kami Wolfe, Swan, Kelli, Virani, Alice

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