The United States Drug Allergy Registry: A Prospective Longitudinal Cohort Study of Patients Tested for Drug Allergies by Blumenthal, Kimberly, Ramsey, Allison, Samarakoon, Upeka, Otani, Iris, Gonzalez-Estrada, Alexei, Banerji, Aleena, Liu, Anne, Wickner, Paige, Stone, Cosby, Park, Miguel, Mancini, Christian, Judd, Allen, Ahola, Catherine, Fu, Xiaoqing, Zhang, Yuqing, Donelan, Karen, Mustafa, S Shahzad, Blue, Holly, Sheflin, Dawn, Harkness, Tyler, Khan, David, Garzon-Siatoya, Wendy, Morgenstern-Kaplan, Dan, Marks, Madeline, Kerrigan, Amy, Rukasin, Christine, Phillips, Elizabeth

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Targeted sequencing for hereditary breast and ovarian cancer in BRCA1/2-negative families reveals complex genetic architecture and phenocopies by Plowman, Jocelyn N., Matoy, Evanjalina J., Uppala, Lavanya V., Draves, Samantha B., Watson, Cynthia J., Sefranek, Bridget A., Stacey, Mark L., Anderson, Samuel P., Belshan, Michael A., Blue, Elizabeth E., Huff, Chad D., Fu, Yusi, Stessman, Holly A.F.

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In vitro data suggest a role for PMS2 Kozak sequence mutations in Lynch syndrome risk by Matoy, Evanjalina J., Plowman, Jocelyn N., Watson, Cynthia J., Belshan, Michael A., Blue, Elizabeth E., Huff, Chad D., Stessman, Holly A.F.

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Developing an integrated framework for Marine Cultural Heritage (MCH) and Marine Protected Areas (MPA) across Africa and the Middle East by Breen, Colin, Tews, Sophie, Nikolaus, Julia, Ray, Nick, Holly, Georgia, Andreou, Georgia, McGonigle, Chris, Westley, Kieran, Blue, Lucy

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De Novo Mutations in NALCN Cause a Syndrome Characterized by Congenital Contractures of the Limbs and Face, Hypotonia, and Developmental Delay by Chong, Jessica X., McMillin, Margaret J., Shively, Kathryn M., Beck, Anita E., Marvin, Colby T., Armenteros, Jose R., Buckingham, Kati J., Nkinsi, Naomi T., Boyle, Evan A., Berry, Margaret N., Bocian, Maureen, Foulds, Nicola, Uzielli, Maria Luisa Giovannucci, Haldeman-Englert, Chad, Hennekam, Raoul C.M., Kaplan, Paige, Kline, Antonie D., Mercer, Catherine L., Nowaczyk, Malgorzata J.M., Klein Wassink-Ruiter, Jolien S., McPherson, Elizabeth W., Moreno, Regina A., Scheuerle, Angela E., Shashi, Vandana, Stevens, Cathy A., Carey, John C., Monteil, Arnaud, Lory, Philippe, Tabor, Holly K., Smith, Joshua D., Shendure, Jay, Nickerson, Deborah A., Bamshad, Michael J., Shendure, Jay, Nickerson, Deborah A., Abecasis, Gonçalo R., Anderson, Peter, Blue, Elizabeth Marchani, Annable, Marcus, Browning, Brian L., Buckingham, Kati J., Chen, Christina, Chin, Jennifer, Chong, Jessica X., Cooper, Gregory M., Davis, Colleen P., Frazar, Christopher, Harrell, Tanya M., He, Zongxiao, Jain, Preti, Jarvik, Gail P., Jimenez, Guillaume, Johanson, Eric, Jun, Goo, Kircher, Martin, Kolar, Tom, Krauter, Stephanie A., Krumm, Niklas, Leal, Suzanne M., Luksic, Daniel, Marvin, Colby T., McMillin, Margaret J., McGee, Sean, O’Reilly, Patrick, Paeper, Bryan, Patterson, Karynne, Perez, Marcos, Phillips, Sam W., Pijoan, Jessica, Poel, Christa, Reinier, Frederic, Robertson, Peggy D., Santos-Cortez, Regie, Shaffer, Tristan, Shephard, Cindy, Shively, Kathryn M., Siegel, Deborah L., Smith, Joshua D., Staples, Jeffrey C., Tabor, Holly K., Tackett, Monica, Underwood, Jason G., Wegener, Marc, Wang, Gao, Wheeler, Marsha M., Yi, Qian, Bamshad, Michael J.

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Molecular outcomes, clinical consequences, and genetic diagnosis of Oculocutaneous Albinism in Pakistani population by Shahzad, Mohsin, Yousaf, Sairah, Waryah, Yar M., Gul, Hadia, Kausar, Tasleem, Tariq, Nabeela, Mahmood, Umair, Ali, Muhammad, Khan, Muzammil A., Waryah, Ali M., Shaikh, Rehan S., Riazuddin, Saima, Ahmed, Zubair M.

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Autosomal-Dominant Multiple Pterygium Syndrome Is Caused by Mutations in MYH3 by Chong, Jessica X., Burrage, Lindsay C., Beck, Anita E., Marvin, Colby T., McMillin, Margaret J., Shively, Kathryn M., Harrell, Tanya M., Buckingham, Kati J., Bacino, Carlos A., Jain, Mahim, Alanay, Yasemin, Berry, Susan A., Carey, John C., Gibbs, Richard A., Lee, Brendan H., Krakow, Deborah, Shendure, Jay, Nickerson, Deborah A., Bamshad, Michael J., Shendure, Jay, Nickerson, Deborah A., Abecasis, Gonçalo R., Anderson, Peter, Blue, Elizabeth Marchani, Annable, Marcus, Browning, Brian L., Buckingham, Kati J., Chen, Christina, Chin, Jennifer, Chong, Jessica X., Cooper, Gregory M., Davis, Colleen P., Frazar, Christopher, Harrell, Tanya M., He, Zongxiao, Jain, Preti, Jarvik, Gail P., Jimenez, Guillaume, Johanson, Eric, Jun, Goo, Kircher, Martin, Kolar, Tom, Krauter, Stephanie A., Krumm, Niklas, Leal, Suzanne M., Luksic, Daniel, Marvin, Colby T., McMillin, Margaret J., McGee, Sean, O’Reilly, Patrick, Paeper, Bryan, Patterson, Karynne, Perez, Marcos, Phillips, Sam W., Pijoan, Jessica, Poel, Christa, Reinier, Frederic, Robertson, Peggy D., Santos-Cortez, Regie, Shaffer, Tristan, Shephard, Cindy, Shively, Kathryn M., Siegel, Deborah L., Smith, Joshua D., Staples, Jeffrey C., Tabor, Holly K., Tackett, Monica, Underwood, Jason G., Wegener, Marc, Wang, Gao, Wheeler, Marsha M., Yi, Qian, Bamshad, Michael J.

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Abstract NS10: Reducing Readmission Rates Bedside Nursing Led Discharge Rounds by Blue, Jennifer S, Clifton, Diane L, Meinel, Patricia A, Muller, Holly

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Dispelling stereotypes: promoting disability equality through film by Schwartz, Diane, Blue, Elfreda, McDonald, Mary, Giuliani, George, Weber, Genevieve, Seirup, Holly, Rose, Sage, Elkis-Albuhoff, Deborah, Rosenfeld, Jeffrey, Perkins, Andrea

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