Clinical identification of feeding and swallowing disorders in 0–6 month old infants with Down syndrome von Stanley, Maria A., Shepherd, Nicole, Duvall, Nichole, Jenkinson, Sandra B., Jalou, Hasnaa E., Givan, Deborah C., Steele, Gregory H., Davis, Charlene, Bull, Marilyn J., Watkins, Donna U., Roper, Randall J.

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Obstructive sleep apnea in young infants with Down Syndrome evaluated in a Down Syndrome specialty clinic von Goffinski, Alida, Stanley, Maria A., Shepherd, Nicole, Duvall, Nichole, Jenkinson, Sandra B., Davis, Charlene, Bull, Marilyn J., Roper, Randall J.

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Outcomes of the "BRCA Quality Improvement Dissemination Program": An initiative to improve patient receipt of cancer genetics services at five health systems von Bednar, Erica M., Chen, Minxing, Walsh, Michael T., Eppolito, Amanda L., Klein, Molly H., Teed, Kelly, Hodge, Brittany, Hunter, Jordan, Chao, Han Gill, Davis, Dillon, Serchion, Wilshauna, Yobbi, Cara, Krukenberg, Rebekah, Jenkinson, Sandra B., Moore, Jennifer J., Garcia, Cassandra, Gonzalez, Fatimaeliza, Murray, Towanna, Nielsen, Linda D., Ho, Brenda, Haas, Megan, Greenzweig, Sarah B., Anderson, Abby, Johnson, Christina, Morman, Nichole A., Bowdish, Elizabeth, Wise, Emaline, Cooper, Julia N., Russ, Pauline Kefalas, Tondo-Steele, Katelyn, de Gracia, Buonarotti F., Levin, Brooke, Mattie, Kristin, Zarnawski, Kathryn, Kalasinski, Molly, Stone, Jennifer, O'Brien, Caitlin, Bream, Alexa, Kennedy, Aidan M., Paul, Rachel A., Bilbao, Michelle, Romero, Maureen, Carr, Rebecca L., Siettmann, Jennifer M., Vercruyssen, Anna K., Leon, Kaycee, Arun, Banu K., Grainger, Andrew V., Warshal, David P., Bowman, Erin, Goedde, Timothy A., Halaharvi, Deepa, Rath, Kellie, Grana, Generosa, Mina, Lida, Lu, Karen H.

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Creation and Implementation of an Environmental Scan to Assess Cancer Genetics Services at Three Oncology Care Settings von Bednar, Erica M., Walsh, Michael T., Baker, Ellen, Muse, Kimberly I., Oakley, Holly D., Krukenberg, Rebekah C., Dresbold, Cara S., Jenkinson, Sandra B., Eppolito, Amanda L., Teed, Kelly B., Klein, Molly H., Morman, Nichole A., Bowdish, Elizabeth C., Russ, Pauline, Wise, Emaline E., Cooper, Julia N., Method, Michael W., Henson, John W., Grainger, Andrew V., Arun, Banu K., Lu, Karen H.

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DICER1 syndrome: clarifying the diagnosis, clinical features and management implications of a pleiotropic tumour predisposition syndrome von Slade, Ingrid, Bacchelli, Chiara, Davies, Helen, Murray, Anne, Abbaszadeh, Fatemeh, Hanks, Sandra, Barfoot, Rita, Burke, Amos, Chisholm, Julia, Hewitt, Martin, Jenkinson, Helen, King, Derek, Morland, Bruce, Pizer, Barry, Prescott, Katrina, Saggar, Anand, Side, Lucy, Traunecker, Heidi, Vaidya, Sucheta, Ward, Paul, Futreal, P Andrew, Vujanic, Gordan, Nicholson, Andrew G, Sebire, Neil, Turnbull, Clare, Priest, John R, Pritchard-Jones, Kathryn, Houlston, Richard, Stiller, Charles, Stratton, Michael R, Douglas, Jenny, Rahman, Nazneen

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Targeting ASIC1 in primary progressive multiple sclerosis: evidence of neuroprotection with amiloride von ARUN, Tarunya, TOMASSINI, Valentina, FUGGER, Lars, ROVIRA, Alex, JENKINSON, Mark, PALACE, Jacqueline, SBARDELLA, Emilia, DE RUITER, Michiel B, MATTHEWS, Lucy, ISABEL LEITE, Maria, GELINEAU-MOREL, Rose, CAVEY, Ana, VERGO, Sandra, CRANER, Matt

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Histopathology Is Key to Interpreting Multiplex Molecular Test Results From Postmortem Minimally Invasive Tissue Samples von Ritter, Jana M., Seixas, Josilene N., Walong, Edwin, Dawa, Jeanette, Onyango, Clayton, Pimenta, Fabiana C., Carvalho, Maria da Gloria, Silva-Flannery, Luciana, Jenkinson, Tiffany, Howard, Katie, Bhatnagar, Julu, Diaz, Maureen, Winchell, Jonas M., Zaki, Sherif R., Chaves, Sandra S., Martines, Roosecelis B.

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Outcomes of the BRCA quality improvement dissemination program in three health systems von Bednar, Erica M., Chen, Minxing, Walsh, Michael T., Eppolito, Amanda L., Teed, Kelly B., Klein, Molly H., Chao, Han, Berg, Jordan, Bowman, Erin, Yobbi, Cara S., Krukenberg, Rebekah C., Jenkinson, Sandra, Moore, Jennifer, Garcia, Cassie, Goedde, Timothy, Morman, Nichole A., Bowdish, Elizabeth C., Wise, Emaline, Rath, Kellie S., Lu, Karen H.

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Gaze2Segment: A Pilot Study for Integrating Eye-Tracking Technology into Medical Image Segmentation von Khosravan, Naji, Celik, Haydar, Turkbey, Baris, Cheng, Ruida, McCreedy, Evan, McAuliffe, Matthew, Bednarova, Sandra, Jones, Elizabeth, Chen, Xinjian, Choyke, Peter, Wood, Bradford, Bagci, Ulas

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Bi-allelic variants in the mitochondrial RNase P subunit PRORP cause mitochondrial tRNA processing defects and pleiotropic multisystem presentations von Hochberg, Irit, Demain, Leigh A. M, Richer, Julie, Thompson, Kyle, Urquhart, Jill E, Rea, Alessandro, Pagarkar, Waheeda, Rodríguez Palmero, Agustí, Schlüter, Agatha, Verdura, Edgard, Pujol, Aurora, Quijada Fraile, Pilar, Amberger, Albert, Deutschmann, Andrea J, Demetz, Sandra, Gillespie, Meredith, Belyantseva, Inna A, Mcmillan, Hugh J, Barzik, Melanie, Beaman, Glenda M, Motha, Reeya, Ng, Kah Ying, O’sullivan, James, Williams, Simon G, Bhaskar, Sanjeev S, Lawrence, Isabella R, Jenkinson, Emma M, Zambonin, Jessica L, Blumenfeld, Zeev, Yalonetsky, Sergey, Oerum, Stephanie, Rossmanith, Walter, Yue, Wyatt W, Zschocke, Johannes, Munro, Kevin J, Battersby, Brendan J, Friedman, Thomas B, Taylor, Robert W, O’keefe, Raymond T, Newman, William G

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Bi-allelic variants in the mitochondrial RNase P subunit PRORP cause mitochondrial tRNA processing defects and pleiotropic multisystem presentations von Hochberg, Irit, Demain, Leigh A. M, Richer, Julie, Thompson, Kyle, Urquhart, Jill E, Rea, Alessandro, Pagarkar, Waheeda, Rodríguez-Palmero, Agustí, Schlüter, Agatha, Verdura, Edgard, Pujol, Aurora, Quijada-Fraile, Pilar, Amberger, Albert, Deutschmann, Andrea J, Demetz, Sandra, Gillespie, Meredith, Belyantseva, Inna A, McMillan, Hugh J, Barzik, Melanie, Beaman, Glenda M, Motha, Reeya, Ng, Kah Ying, O'Sullivan, James, Williams, Simon G, Bhaskar, Sanjeev S, Lawrence, Isabella R, Jenkinson, Emma M, Zambonin, Jessica L, Blumenfeld, Zeev, Yalonetsky, Sergey, Oerum, Stephanie, Rossmanith, Walter, Yue, Wyatt W, Zschocke, Johannes, Munro, Kevin J, Battersby, Brendan J, Friedman, Thomas B, Taylor, Robert W, O'Keefe, Raymond T, Newman, William G

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Bi-allelic variants in the mitochondrial RNase P subunit PRORP cause mitochondrial tRNA processing defects and pleiotropic multisystem presentations von Hochberg, Irit, Demain, Leigh A. M, Richer, Julie, Thompson, Kyle, Urquhart, Jill E, Rea, Alessandro, Pagarkar, Waheeda, Rodríguez-Palmero, Agustí, Schlüter, Agatha, Verdura, Edgard, Pujol, Aurora, Quijada-Fraile, Pilar, Amberger, Albert, Deutschmann, Andrea J, Demetz, Sandra, Gillespie, Meredith, Belyantseva, Inna A, McMillan, Hugh J, Barzik, Melanie, Beaman, Glenda M, Motha, Reeya, Ng, Kah Ying, O'Sullivan, James, Williams, Simon G, Bhaskar, Sanjeev S, Lawrence, Isabella R, Jenkinson, Emma M, Zambonin, Jessica L, Blumenfeld, Zeev, Yalonetsky, Sergey, Oerum, Stephanie, Rossmanith, Walter, Yue, Wyatt W, Zschocke, Johannes, Munro, Kevin J, Battersby, Brendan J, Friedman, Thomas B, Taylor, Robert W, O'Keefe, Raymond T, Newman, William G

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