Reduced Uptake of Family Screening in Genotype-Negative Versus Genotype-Positive Long QT Syndrome von Hanninen, Mikael, Klein, George J., Laksman, Zachary, Conacher, Susan S., Skanes, Allan C., Yee, Raymond, Gula, Lorne J., Leong-Sit, Peter, Manlucu, Jaimie, Krahn, Andrew D.

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Early repolarization is associated with symptoms in patients with type 1 and type 2 long QT syndrome von Laksman, Zachary W.M., MD, Gula, Lorne J., MD, FHRS, Saklani, Pradyot, MD, Cassagneau, Romain, MD, Steinberg, Christian, MD, Conacher, Susan, MSc, Yee, Raymond, MD, FHRS, Skanes, Allan, MD, Leong-Sit, Peter, MD, FHRS, Manlucu, Jaimie, MD, Klein, George J., MD, Krahn, Andrew D., MD, FHRS

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A Detailed Description and Assessment of Outcomes of Patients With Hospital Recorded QTc Prolongation von Laksman, Zachary, MD, Momciu, Bogdan, MD, Seong, You Won, Burrows, Patricia, RCT, Conacher, Susan, MSc, Manlucu, Jaimie, MD, Leong-Sit, Peter, MD, Gula, Lorne J., MD, Skanes, Allan C., MD, Yee, Raymond, MD, Klein, George J., MD, Krahn, Andrew D., MD

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Arrhythmogenic Right Ventricular Cardiomyopathy With Recessive Inheritance Related to a New Homozygous Desmocollin-2 Mutation von Al-Sabeq, Basil, MD, Krahn, Andrew D., MD, FRCPC, Conacher, Susan, MSc, Klein, George J., MD, FRCPC, Laksman, Zachary, MD, FRCPC

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Babies in occiput posterior position are significantly more likely to require an emergency cesarean birth compared with babies in occiput transverse position in the second stage of... von Tempest, Nicola, Lane, Steven, Hapangama, Dharani, Bassel, Wattar, Jennifer, Tamblyn, William, Parry‐Smith, Matthew, Prior, Dhivya, Chandrasekaran, Shailly Sahu, Bansali, Geethanjali, Boregowda, Fulva, Dave, Julie, Guiver, Mohita, Gupta, Cecilia, Iyasere, Kate, Jones, Vijaya, Karanam, Jessica, Player, Daxina, Bhatt, Zoe, Boyes, Ciara, Carpenter, Helen, Clarke, Trent, Corr, Sarah, Dauleh, Jemma, Egan, Smitha, George, Phillipa, Harris, Robbie, Kerr, Nira, Ramachandran, Jennifer, Ramage, Rachel, Tildesley, Ferdousi, Akhter, Anna, McDougall, Obi, Ojukwu, Katarina, Tvarozkova, Nicola, Ramshaw, Michelle, Creed, Kate, Danby, Rosie, Grainger, Aiste, McCormick, Melissa, Pearce, Ruth, Thompson, Simon, Williams, Alison, Wonnacott, Jemma, Yorke, Atiyah, Kamran, Jandy, Fernandes, Lamia, Zafrani, Angus, Conacher, Dina, Tannous, Susan, Tracey, Louisa, Manning, Alex, Bain, Jessica, Braschi, Alexandra, Dehnel, Sayaka, Okano, Eleanor, Rayner, Fiona, Day, Alaa, Abdou, Sarah, Channing, Samantha, Jones, Tipswalo, Day, Noreen, Haque, Kiran, Jilani, Angharad, Jones, Lisa, Pilkington, Cath, Stone, Caryl, Thomas, Janet, Berry, Margaret, Perumalla, Catherine, Johnston, Sarah, Smyth, Grisham, Smotra, Kamana, Subba, Mausumi, Ghosh, Nidhi, Gulati, Sarra, Merzougui, Chimwemwe, Miti, Mohammad, Mohamed, Yulia, Nicholson, Radhae, Raghavan, Camille, Smyth, Helen, Stevenson, Nasreen, Syeda, Alex, Tan, Laura, Veal, Rabia, Zahid, Sheethal, Madari, Claire, McCormack, Catriona, Barlow, Laura, Beatty, Anusha, D’Sa, Fiona, Hendry, Victoria, McAlpine‐Scott, Daniel, Short, John, Dalton, Sarah, Cartland, Sudeepthi, Kakara, Tom, Pettinger, Malcolm, Scott, James, Tibbott

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Loss-of-Function KCNE2 Variants: True Monogenic Culprits of Long-QT Syndrome or Proarrhythmic Variants Requiring Secondary Provocation? von Roberts, Jason D, Krahn, Andrew D, Ackerman, Michael J, Rohatgi, Ram K, Moss, Arthur J, Nazer, Babak, Tadros, Rafik, Gerull, Brenda, Sanatani, Shubhayan, Wijeyeratne, Yanushi D, Baruteau, Alban-Elouen, Muir, Alison R, Pang, Benjamin, Cadrin-Tourigny, Julia, Talajic, Mario, Rivard, Lena, Tester, David J, Liu, Taylor, Whitman, Isaac R, Wojciak, Julianne, Conacher, Susan, Gula, Lorne J, Leong-Sit, Peter, Manlucu, Jaimie, Green, Martin S, Hamilton, Robert, Healey, Jeff S, Lopes, Coeli M, Behr, Elijah R, Wilde, Arthur A, Gollob, Michael H, Scheinman, Melvin M

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ALU transposition induces familial hypertrophic cardiomyopathy von Nfonsam, Landry, Huang, Lijia, Carson, Nancy, McGowan‐Jordan, Jean, Beaulieu Bergeron, Melanie, Goobie, Sharan, Conacher, Susan, McCarty, David, Benson, Lee, Hewson, Stacy, Zahavich, Laura, Sinclair‐Bourque, Elizabeth, Smith, Amanda, Potter, Ryan, Ghani, Mahdi, Bronicki, Lucas, Jarinova, Olga

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A large familial pathogenic Plakophilin-2 gene (PKP2) deletion manifesting with sudden cardiac death and lone atrial fibrillation: Evidence for alternating atrial and ventricular p... von Alhassani, Saad, Deif, Bishoy, Conacher, Susan, Cunningham, Kristopher S., Roberts, Jason D.

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KCNJ2 Variant of Unknown Significance Reclassified as Long QT Syndrome Causing Ventricular Fibrillation von Obeyesekere, Manoj N., MBBS, Klein, George J., MD, Conacher, Susan, MSc, Krahn, Andrew D., MD, FHRS

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Pregnancy in Catecholaminergic Polymorphic Ventricular Tachycardia von Cheung, Christopher C., Lieve, Krystien V., Roston, Thomas M., van der Ree, Martijn H., Deyell, Marc W., Andrade, Jason G., Laksman, Zachary W., Nannenberg, Eline A., Tadros, Rafik, Pang, Benjamin, Rutberg, Julie, Green, Martin S., Conacher, Susan, Seifer, Colette M., Roberts, Jason D., Steinberg, Christian, Sanatani, Shubhayan, Wilde, Arthur A., Krahn, Andrew D.

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End-Recovery QTc: A Useful Metric for Assessing Genetic Variants of Unknown Significance in Long-QT syndrome von OBEYESEKERE, MANOJ N., SY, RAYMOND W., KLEIN, GEORGE J., GULA, LORNE J., MODI, SIMON, CONACHER, SUSAN, LEONG-SIT, PETER, SKANES, ALLAN C., YEE, RAYMOND, KRAHN, ANDREW D.

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622 Outcome of fetuses with increased nuchal translucency and normal karyotypes von Winsor, Stephanie, Conacher, Susan, Chitayat, David, Johnson, Joan

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The effects of prenatal group genetic counselling on knowledge, anxiety and decisional conflict: issues for nuchal translucency screening von Kaiser, Amy S., Ferris, Lorraine E., Pastuszak, Anne L., Llewellyn-Thomas, Hilary, Johnson, Jo-Ann, Conacher, Susan, Shaw, B. F.

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A large familial pathogenic Plakophilin-2 gene (PKP2) deletion manifesting with sudden cardiac death and lone atrial fibrillation: Evidence for alternating atrial and ventricular p... von Alhassani, Saad, Deif, Bishoy, Conacher, Susan, Cunningham, Kristopher S, Roberts, Jason D

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