Recurrent pneumothorax in a case of tenascin‐X deficient Ehlers–Danlos syndrome: Broadening the phenotypic spectrum by Santoreneos, Renee, Vakulin, Cassandra, Ellul, Melissa, Rawlings, Lesley, Hardy, Tristan, Poplawski, Nicola

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Recurrent pneumothorax in a case of t enascin‐X deficient Ehlers–Danlos syndrome: Broadening the phenotypic spectrum by Santoreneos, Renee, Vakulin, Cassandra, Ellul, Melissa, Rawlings, Lesley, Hardy, Tristan, Poplawski, Nicola

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DCTA triplets: a fascinating trip by Phan, Jennifer, DeJong, Lucas, Kassahn, Karin, Vakulin, Cassandra, Simsek, Aygul, Rawlings, Lesley, Dubowsky, Andrew, Waters, Wendy, Yu, Sui, Hardy, Tristan

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Shariant platform: Enabling evidence sharing across Australian clinical genetic-testing laboratories to support variant interpretation by Tudini, Emma, Andrews, James, Lawrence, David M., King-Smith, Sarah L., Baker, Naomi, Baxter, Leanne, Beilby, John, Bennetts, Bruce, Beshay, Victoria, Black, Michael, Boughtwood, Tiffany F., Brion, Kristian, Cheong, Pak Leng, Christie, Michael, Christodoulou, John, Cox, Kathy, Davis, Mark R., Dejong, Lucas, Dinger, Marcel E., Doig, Kenneth D., Douglas, Evelyn, Dubowsky, Andrew, Ellul, Melissa, Fellowes, Andrew, Fisk, Katrina, Fortuno, Cristina, Friend, Kathryn, Gallagher, Renee L., Gao, Song, Hackett, Emma, Hadler, Johanna, Hipwell, Michael, Ho, Gladys, Hollway, Georgina, Hooper, Amanda J., Kassahn, Karin S., Krishnaraj, Rahul, Lau, Chiyan, Le, Huong, San Leong, Huei, Lundie, Ben, Lunke, Sebastian, Marty, Anthony, McPhillips, Mary, Nguyen, Lan T., Nones, Katia, Palmer, Kristen, Pearson, John V., Quinn, Michael C.J., Rawlings, Lesley H., Sadedin, Simon, Sanchez, Louisa, Schreiber, Andreas W., Sigalas, Emanouil, Simsek, Aygul, Soubrier, Julien, Stark, Zornitza, Thompson, Bryony A., U, James, Vakulin, Cassandra G., Wells, Amanda V., Wise, Cheryl A., Woods, Rick, Ziolkowski, Andrew, Brion, Marie-Jo, Scott, Hamish S., Thorne, Natalie P., Spurdle, Amanda B., Akesson, Lauren, Allcock, Richard, Ashton, Katie, Bell, Damon A., Brown, Anna, Buckley, Michael, Burrows, Linda, Byrne, Alicia, Chan, Eva, Cliffe, Corrina, Clifton-Bligh, Roderick, Dooley, Susan, Fernandez, Miriam Fanjul, Farnsworth, Elizabeth, Ha, Thuong, Henry, Denae, Holds, Duncan, Holman, Katherine, Jackson, Matilda, Kang, Sinlay, Luxford, Catherine, McManus, Sam, Mehrtens, Rachael, Meldrum, Cliff, Pantaleo, Sarah-Jane, Phelan, Dean, Pontikinas, Electra, Ravine, Anja, Roscioli, Tony, Scott, Rodney, Simons, Keryn, Vanwageningen, Oliver

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RUNX1-mutated families show phenotype heterogeneity and a somatic mutation profile unique to germline predisposed AML by Brown, Anna L., Arts, Peer, Carmichael, Catherine L., Babic, Milena, Dobbins, Julia, Chong, Chan-Eng, Schreiber, Andreas W., Feng, Jinghua, Phillips, Kerry, Wang, Paul P.S., Ha, Thuong, Homan, Claire C., King-Smith, Sarah L., Rawlings, Lesley, Vakulin, Cassandra, Dubowsky, Andrew, Burdett, Jessica, Moore, Sarah, McKavanagh, Grace, Henry, Denae, Wells, Amanda, Mercorella, Belinda, Nicola, Mario, Suttle, Jeffrey, Wilkins, Ella, Li, Xiao-Chun, Michaud, Joelle, Brautigan, Peter, Cannon, Ping, Altree, Meryl, Jaensch, Louise, Fine, Miriam, Butcher, Carolyn, D'Andrea, Richard J., Lewis, Ian D., Hiwase, Devendra K., Papaemmanuil, Elli, Horwitz, Marshall S., Natsoulis, Georges, Rienhoff, Hugh Y., Patton, Nigel, Mapp, Sally, Susman, Rachel, Morgan, Susan, Cooney, Julian, Currie, Mark, Popat, Uday, Bochtler, Tilmann, Izraeli, Shai, Bradstock, Kenneth, Godley, Lucy A., Krämer, Alwin, Fröhling, Stefan, Wei, Andrew H., Forsyth, Cecily, Mar Fan, Helen, Poplawski, Nicola K., Hahn, Christopher N., Scott, Hamish S.

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RNF43 pathogenic Germline variant in a family with colorectal cancer by Mikaeel, Reger R., Young, Joanne P., Li, Yun, Poplawski, Nicola K., Smith, Eric, Horsnell, Mehgan, Uylaki, Wendy, Tomita, Yoko, Townsend, Amanda R., Feng, Jinghua, Zibat, Arne, Kaulfuß, Silke, Müller, Christian, Yigit, Gökhan, Wollnik, Bernd, Scott, Hamish, Rawlings, Lesley, Henry, Denae, Vakulin, Cassandra, Dubowsky, Andrew, Price, Timothy J.

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Unraveling facets of MECOM-associated syndrome: somatic genetic rescue, clonal hematopoiesis, and phenotype expansion by Venugopal, Parvathy, Arts, Peer, Fox, Lucy C., Simons, Annet, Hiwase, Devendra K., Bardy, Peter G., Swift, Annette, Ross, David M., van Vulpen, Lize F. D., Buijs, Arjan, Bolton, Kelly L., Getta, Bartlomiej, Furlong, Eliska, Carter, Tina, Krapels, Ingrid, Hoeks, Marlijn, Al Kindy, Adila, Al Kindy, Farah, de Munnik, Sonja, Evans, Pamela, Frank, Mahalia S. B., Bournazos, Adam M., Cooper, Sandra T., Ha, Thuong Thi, Jackson, Matilda R., Arriola-Martinez, Luis, Phillips, Kerry, Brennan, Yvonne, Bakshi, Madhura, Ambler, Karen, Gao, Song, Kassahn, Karin S., Kenyon, Rosalie, Hung, Kevin, Babic, Milena, McGovern, Alan, Rawlings, Lesley, Vakulin, Cassandra, Dejong, Lucas, Fathi, Rema, McRae, Simon, Myles, Nicholas, Ladon, Dariusz, Jongmans, Marjolijn, Kuiper, Roland P., Poplawski, Nicola K., Barbaro, Pasquale, Blombery, Piers, Brown, Anna L., Hahn, Christopher N., Scott, Hamish S.

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Expanded Phenotypic and Genetic Heterogeneity in the Clinical Spectrum of FPD-AML: Lymphoid Malignancies and Skin Disorders Are Common Features in Carriers of Germline RUNX1 Mutati... by Brown, Anna L, Hahn, Christopher N, Carmichael, Catherine, Wilkins, Ella, Babic, Milena, Chong, Chan-Eng, Li, Xiao-Chun, Michaud, Joelle, Cannon, Ping, Poplawski, Nicola, Altree, Meryl, Phillips, Kerry, Jaensch, Louise, Fine, Miriam, Schreiber, Andreas W, Feng, Jinghua, Rawlings, Lesley, Vakulin, Cassandra, Butcher, Carolyn, D'Andrea, Richard, Lewis, Ian D, Patton, Nigel, Forsyth, Cecily, Mapp, Sally, Mar Fan, Helen, Susman, Rachel, Morgan, Sue, Cooney, Julian, Currie, Mark S, Popat, Uday R., Bradstock, Kenneth, Sorrell, April D., Owen, Carolyn J., Horwitz, Marshall S, Hiwase, Devendra, Krämer, Alwin, Fröhling, Stefan, Godley, Lucy A, Churpek, Jane E, Scott, Hamish S

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Recurrent pneumothorax in a case of tenascin-X deficient Ehlers-Danlos syndrome: Broadening the phenotypic spectrum by Santoreneos, Renee, Vakulin, Cassandra, Ellul, Melissa, Rawlings, Lesley, Hardy, Tristan, Poplawski, Nicola

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