SCN5A mutations in 442 neonates and children: genotype–phenotype correlation and identification of higher-risk subgroups von Baruteau, Alban-Elouen, Kyndt, Florence, Behr, Elijah R, Vink, Arja S, Lachaud, Matthias, Joong, Anna, Schott, Jean-Jacques, Horie, Minoru, Denjoy, Isabelle, Crotti, Lia, Shimizu, Wataru, Bos, Johan M, Stephenson, Elizabeth A, Wong, Leonie, Abrams, Dominic J, Davis, Andrew M, Winbo, Annika, Dubin, Anne M, Sanatani, Shubhayan, Liberman, Leonardo, Kaski, Juan Pablo, Rudic, Boris, Kwok, Sit Yee, Rieubland, Claudine, Tfelt-Hansen, Jacob, Van Hare, George F, Guyomarc’h-Delasalle, Béatrice, Blom, Nico A, Wijeyeratne, Yanushi D, Gourraud, Jean-Baptiste, Le Marec, Hervé, Ozawa, Junichi, Fressart, Véronique, Lupoglazoff, Jean-Marc, Dagradi, Federica, Spazzolini, Carla, Aiba, Takeshi, Tester, David J, Zahavich, Laura A, Beauséjour-Ladouceur, Virginie, Jadhav, Mangesh, Skinner, Jonathan R, Franciosi, Sonia, Krahn, Andrew D, Abdelsayed, Mena, Ruben, Peter C, Yung, Tak-Cheung, Ackerman, Michael J, Wilde, Arthur A, Schwartz, Peter J, Probst, Vincent

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Use of Clinical Exome Sequencing in Isolated Congenital Heart Disease von Zahavich, Laura, Bowdin, Sarah, Mital, Seema

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P342: Loss of function variants in ACTN2 in pediatric patients with infantile-onset dilated cardiomyopathy von Zahavich, Laura, MacPherson, Samantha, Jeewa, Aamir, Jobling, Rebekah

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Mutations in TOP3A Cause a Bloom Syndrome-like Disorder von Martin, Carol-Anne, Sarlós, Kata, Logan, Clare V., Thakur, Roshan Singh, Parry, David A., Bizard, Anna H., Leitch, Andrea, Cleal, Louise, Ali, Nadia Shaukat, Al-Owain, Mohammed A., Allen, William, Altmüller, Janine, Aza-Carmona, Miriam, Barakat, Bushra A.Y., Barraza-García, Jimena, Begtrup, Amber, Bogliolo, Massimo, Cho, Megan T., Cruz-Rojo, Jaime, Dhahrabi, Hassan Ali Mundi, Elcioglu, Nursel H., Gorman, Gráinne S., Jobling, Rebekah, Kesterton, Ian, Kishita, Yoshihito, Kohda, Masakazu, Le Quesne Stabej, Polona, Malallah, Asam Jassim, Nürnberg, Peter, Ohtake, Akira, Okazaki, Yasushi, Pujol, Roser, Ramirez, Maria José, Revah-Politi, Anya, Shimura, Masaru, Stevens, Paul, Taylor, Robert W., Turner, Lesley, Williams, Hywel, Wilson, Carolyn, Yigit, Gökhan, Zahavich, Laura, Alkuraya, Fowzan S., Surralles, Jordi, Iglesias, Alejandro, Murayama, Kei, Wollnik, Bernd, Dattani, Mehul, Heath, Karen E., Hickson, Ian D., Jackson, Andrew P.

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Heart Failure with Recovered Ejection Fraction in Patients with Vinculin Loss-of-function Variants von Zahavich, Laura, Akilen, Rajadurai, George, Kristen, Mital, Seema

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Family screening for hypertrophic cardiomyopathy: Is it time to change practice guidelines? von Lafreniere-Roula, Myriam, Bolkier, Yoav, Zahavich, Laura, Mathew, Jacob, George, Kristen, Wilson, Judith, Stephenson, Elizabeth A, Benson, Leland N, Manlhiot, Cedric, Mital, Seema

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Barriers in applying to genetic counseling Master's degree programs: Perceptions of prospective applicants when compared with Canadian admissions committee members von Zahavich, Laura, Babul‐Hirji, Riyana

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Exercise-Induced Cardiac Arrest in a Child: A Case Report von Katz-Dana, Hadas, Lekchuensakul, Sarin, Hamilton, Robert, Zahavich, Laura, Jobling, Rebekah K, Ratnapalan, Savithiri

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Return of genetic and genomic research findings: experience of a pediatric biorepository von Papaz, Tanya, Liston, Eriskay, Zahavich, Laura, Stavropoulos, Dimitri J, Jobling, Rebekah K, Kim, Raymond H, Reuter, Miriam, Miron, Anastasia, Oechslin, Erwin, Mondal, Tapas, Bergin, Lynn, Smythe, John F, Altamirano-Diaz, Luis, Lougheed, Jane, Yao, Roderick, Akinrinade, Oyediran, Breckpot, Jeroen, Mital, Seema

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Development and Evaluation of Decision Aids to Guide Families’ Predictive Testing Choices for Children at Risk for Arrhythmia or Cardiomyopathy von Christian, Susan, Welsh, Alicia, Yetman, Jeremy, Birch, Patrician, Bartels, Kirsten, Burnell, Lindsay, Curtis, Fiona, Huculak, Cathleen, Zahavich, Laura, Arbour, Laura, Marcadier, Julien, Atallah, Joseph

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Expanding the phenotypic spectrum of NOTCH1 variants: clinical manifestations in families with congenital heart disease von Stanley, Kaitlin J, Kalbfleisch, Kelsey J, Moran, Olivia M, Chaturvedi, Rajiv R, Roifman, Maian, Chen, Xin, Manshaei, Roozbeh, Martin, Nicole, McDermott, Simina, McNiven, Vanda, Myles-Reid, Diane, Nield, Lynne E, Reuter, Miriam S, Schwartz, Marci L B, Shannon, Patrick, Silver, Rachel, Somerville, Cherith, Teitelbaum, Ronni, Zahavich, Laura, Bassett, Anne S, Kim, Raymond H, Mital, Seema, Chitayat, David, Jobling, Rebekah K

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Mutations in TOP3A Cause a Bloom Syndrome-like Disorder von Martin, Carol-Anne, Sarlós, Kata, Logan, Clare V., Thakur, Roshan Singh, Parry, David A., Bizard, Anna H., Leitch, Andrea, Cleal, Louise, Ali, Nadia Shaukat, Al-Owain, Mohammed A., Allen, William, Altmüller, Janine, Aza-Carmona, Miriam, Barakat, Bushra A.Y., Barraza-García, Jimena, Begtrup, Amber, Bogliolo, Massimo, Cho, Megan T., Cruz-Rojo, Jaime, Mundi Dhahrabi, Hassan Ali, Elcioglu, Nursel H., GOSgene, Gorman, Gráinne S., Jobling, Rebekah, Kesterton, Ian, Kishita, Yoshihito, Kohda, Masakazu, Le Quesne Stabej, Polona, Malallah, Asam Jassim, Nürnberg, Peter, Ohtake, Akira, Okazaki, Yasushi, Pujol, Roser, Ramirez, Maria José, Revah-Politi, Anya, Shimura, Masaru, Stevens, Paul, Taylor, Robert W., Turner, Lesley, Williams, Hywel, Wilson, Carolyn, Yigit, Gökhan, Zahavich, Laura, Alkuraya, Fowzan S., Surralles, Jordi, Iglesias, Alejandro, Murayama, Kei, Wollnik, Bernd, Dattani, Mehul, Heath, Karen E., Hickson, Ian D., Jackson, Andrew P.

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Novel Association of a De Novo CALM2 Mutation With Long QT Syndrome and Hypertrophic Cardiomyopathy von Zahavich, Laura, Tarnopolsky, Mark, Yao, Roderick, Mital, Seema

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Return of Results Policies for Genomic Research: Current Practices and the Hearts in Rhythm Organization (HiRO) Approach von Comber, Drake A., Davies, Brianna, Roberts, Jason D., Tadros, Rafik, Green, Martin S., Healey, Jeffrey S., Simpson, Christopher S., Sanatani, Shubhayan, Steinberg, Christian, MacIntyre, Ciorsti, Angaran, Paul, Duff, Henry, Hamilton, Robert, Arbour, Laura, Leather, Richard, Seifer, Colette, Fournier, Anne, Atallah, Joseph, Kimber, Shane, Makanjee, Bhavanesh, Alqarawi, Wael, Cadrin-Tourigny, Julia, Joza, Jacqueline, Gibbs, Karen, Robb, Laura, Zahavich, Laura, Gardner, Martin, Talajic, Mario, Virani, Alice, Krahn, Andrew D., Lehman, Anna, Laksman, Zachary W.M.

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Abstract 14706: Cardiac Phenotype in Children Undergoing Screening for Familial Hypertrophic Cardiomyopathy: Is it Time to Change Screening Guidelines? von Zahavich, Laura, Mathew, Jacob, Wilson, Judith, George, Kristen, Bowdin, Sarah, Benson, Leland N, Mital, Seema

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Exploring Barriers and Facilitators to Indirect Cascade Screening for Familial Hypercholesteraemia in a Paediatric/Parent Population von Dickson, Megan A., Zahavich, Laura, Rush, Janet, Hewson, Stacy, Chitayat, David, McCrindle, Brian W., Chahal, Nita

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“Acquired” Brugada syndrome in a cardiac allograft von Power, Alyssa, Lynch, Áine, Zahavich, Laura, Lévesque, Sébastien A., Stephenson, Elizabeth A., Jean‐St‐Michel, Emilie, Dipchand, Anne I., Jeewa, Aamir

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Adverse early life events are not associated with pediatric multiple sclerosis (MS) (P3.217) von Freitas, Cassandra, O’Mahony, Julia, Zahavich, Laura, Guimond, Colleen, Yeh, E. Ann, Arnold, Douglas, Bar-Or, Amit, Sadovnick, Dessa, Marrie, Ruth-Ann, Banwell, Brenda

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Mutations in TOP3A Cause a Bloom Syndrome-like Disorder von Martin, Carol-Anne, Sarlós, Kata, Logan, Clare V., Thakur, Roshan Singh, Parry, David A., Bizard, Anna H., Leitch, Andrea, Cleal, Louise, Ali, Nadia Shaukat, Al-Owain, Mohammed A., Allen, William, Altmüller, Janine, Aza-Carmona, Miriam, Barakat, Bushra A.Y., Barraza-García, Jimena, Begtrup, Amber, Bogliolo, Massimo, Cho, Megan T., Cruz-Rojo, Jaime, Dhahrabi, Hassan Ali Mundi, Elcioglu, Nursel H., Gorman, Gráinne S., Jobling, Rebekah, Kesterton, Ian, Kishita, Yoshihito, Kohda, Masakazu, Le Quesne Stabej, Polona, Malallah, Asam Jassim, Nürnberg, Peter, Ohtake, Akira, Okazaki, Yasushi, Pujol, Roser, Ramirez, Maria José, Revah-Politi, Anya, Shimura, Masaru, Stevens, Paul, Taylor, Robert W., Turner, Lesley, Williams, Hywel, Wilson, Carolyn, Yigit, Gökhan, Zahavich, Laura, Alkuraya, Fowzan S., Surralles, Jordi, Iglesias, Alejandro, Murayama, Kei, Wollnik, Bernd, Dattani, Mehul, Heath, Karen E., Hickson, Ian D., Jackson, Andrew P.

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Return of genetic and genomic research findings: experience of a pediatric biorepository von Papaz, Tanya, Liston, Eriskay, Zahavich, Laura, Stavropoulos, Dimitri J, Jobling, Rebekah K, Kim, Raymond H, Reuter, Miriam, Miron, Anastasia, Oechslin, Erwin, Mondal, Tapas, Bergin, Lynn, Smythe, John F, Altamirano-Diaz, Luis, Lougheed, Jane, Yao, Roderick, Akinrinade, Oyediran, Breckpot, Jeroen, Mital, Seema

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