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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Power and powerlessness in a pandemic by Fine-Goulden, Miriam R.

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A novel germline SAMD9L mutation in a family with ataxia-pancytopenia syndrome and pediatric acute lymphoblastic leukemia by Cheah, Jesse J C, Brown, Anna L, Schreiber, Andreas W, Feng, Jinghua, Babic, Milena, Moore, Sarah, Young, Chun-Chun, Fine, Miriam, Phillips, Kerry, Guandalini, Michael, Wilson, Peter, Poplawski, Nicola, Hahn, Christopher N, Scott, Hamish S

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Self-reverting mutations partially correct the blood phenotype in a Diamond Blackfan anemia patient by Venugopal, Parvathy, Moore, Sarah, Lawrence, David M, George, Amee J, Hannan, Ross D, Bray, Sarah Ce, To, Luen Bik, D'Andrea, Richard J, Feng, Jinghua, Tirimacco, Amanda, Yeoman, Alexandra L, Young, Chun Chun, Fine, Miriam, Schreiber, Andreas W, Hahn, Christopher N, Barnett, Christopher, Saxon, Ben, Scott, Hamish S

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Impact of national guidelines on use of BRCA1/2 germline testing, risk management advice given to women with pathogenic BRCA1/2 variants and uptake of advice by Meiser, Bettina, Kaur, Rajneesh, Morrow, April, Peate, Michelle, Wong, W K Tim, McPike, Emily, Cops, Elisa, Nichols, Cassandra, Austin, Rachel, Fine, Miriam, Thrupp, Letitia, Ward, Robyn, Macrae, Finlay, Hiller, Janet E, Trainer, Alison H, Mitchell, Gillian

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Mechanisms of ventilator dependence in children with neuromuscular and respiratory control disorders identified by monitoring diaphragm electrical activity by Fine-Goulden, Miriam R., Puppala, Naga K., Durward, Andrew

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Novel germ line DDX41 mutations define families with a lower age of MDS/AML onset and lymphoid malignancies by Lewinsohn, Maya, Brown, Anna L., Weinel, Luke M., Phung, Connie, Rafidi, George, Lee, Ming K., Schreiber, Andreas W., Feng, Jinghua, Babic, Milena, Chong, Chan-Eng, Lee, Young, Yong, Agnes, Suthers, Graeme K., Poplawski, Nicola, Altree, Meryl, Phillips, Kerry, Jaensch, Louise, Fine, Miriam, D'Andrea, Richard J., Lewis, Ian D., Medeiros, Bruno C., Pollyea, Daniel A., King, Mary-Claire, Walsh, Tom, Keel, Siobán, Shimamura, Akiko, Godley, Lucy A., Hahn, Christopher N., Churpek, Jane E., Scott, Hamish S.

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776 The effect of the Covid-19 pandemic on the nature of bronchiolitis in infants <6 months admitted to a UK District General Hospital by Smith, Emma, Blyth, Thomas, Fine-Goulden, Miriam

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P62 A review of near infra-red spectroscopy by Donnelly, Peter, Fine-Goulden, Miriam

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An Integrative Genomic Approach to Examine Mutations and Biological Pathways Associated with Hematological Malignancy Development in DDX41 Mutated Families by Venugopal, Parvathy, Cheah, Jesse JC, Eshraghi, Leila, Shahrin, Nur Hezrin, Homan, Claire, Feng, Jinghua, Schreiber, Andreas W, Fine, Miriam, Phillips, Kerry, Poplawski, Nicola, Brown, Anna L, Hahn, Christopher N, Scott, Hamish S

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AN INTEGRATIVE GENOMIC APPROACH TO EXAMINE MUTATIONS AND BIOLOGICAL PATHWAYS ASSOCIATED WITH HAEMATOLOGICAL MALIGNANCY DEVELOPMENT IN DDX41 MUTATED FAMILIES by Cheah, Jesse, Brown, Anna, Eshraghi, Leila, Feng, Jinghua, Schreiber, Andreas, Babic, Milena, Homan, Claire, Fine, Miriam, Philips, Kerry, Poplawski, Nicola, Hahn, Christopher, Scott, Hamish

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Post-COVID-19 paediatric inflammatory multisystem syndrome: association of ethnicity, key worker and socioeconomic status with risk and severity by Broad, Jonathan, Forman, Julia, Brighouse, James, Sobande, Adebola, McIntosh, Alysha, Watterson, Claire, Boot, Elizabeth, Montgomery, Felicity, Gilmour, Iona, Tan, Joy, Fogarty, Mary Johanna, Gomez, Xabier, Cheung, Ronny, Lillie, Jon, Shivamurthy, Vinay, Handforth, Jenny, Miller, Owen, Kenny, Julia, Meesters, Kevin, Martinez-Alier, Nuria, Demirjian, Alicia, Tebruegge, Marc, Alonso, Alejandro, Shah, Tish, White, Marie, Finemore, Anna, Blackburn, Fran, Parish, Emma, Tiesman, Bianca, Trecchi, Nadia, Jackman, John, Butler, Mark, Ramachandran, Rohana, Roueche, Alice, Macaulay, Chloe, Lemer, Claire, Sobande, Debbie, Kamal, Ajanta, Wilkinson, Nick, Arenas, Sara, Christiansen, Nanna, Wan, Mandy, Rashed, Asia, Mathur, Sujeev, Wong, James, Theocharis, Paraskevi, Stewart, Kirsty, Kabir, Saleha, Peacock, Kelly, Pushparajah, Kuberan, Savis, Alex, Regan, Will, Pascall, Emma, Cleary, Aoife, Uy, Mirasol, Heard, Hannah, Carter, Michael, Tibby, Shane, Riphagen, Shelley, MacDougall, Marilyn, Waters, Ben Griffths, Gareth, Minen, Federico, Nyman, Andrew, Goulden, Miriam Fine, MacGruer, Ken, Sa, Mario, Lim, Ming, Bryne, Susan, Cadwgan, Jill, Lim, JP, Singh, Rahul, Tang, Shan, Lumsden, Dan, Senior, Sam, McMurtrie, Sarah, Norridge, Matthew, Emberson, Stephanie, Marr, Stacey, Felton, Victoria, Reid, Chris, Adalat, Shazia, Balasubramanian, Ramnath, Jones, Helen, Alamelu, Jay, Inusa, Baba

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Developing new models of care at speed: learning from healthcare redesign for children with COVID-related multisystem inflammation by Cheung, C Ronny, Finnemore, Anna, Handforth, Jennifer, Bohmer, Richard, Christiansen, Nanna, Miller, Owen, Kenny, Julia, Watterson, Claire, Meesters, Kevin, Fogarty, Mary-Jo, Broad, Jonathan, White, Marie, Blackburn, Frances, Parish, Emma, Tiesman, Bianca, Trecchi, Nadia, Jackman, John, Butler, Mark, Ramachandran, Rohana, Roueche, Alice, Macaulay, Chloe, Montgomery, Felicity, Shivamurthy, Vinay, Wilkinson, Nick, Brighouse, James, Arenas, Sara, Wan, Mandy, Mathur, Sujeev, Wong, James, Theocharis, Paraskevi, Stewart, Kirsty, Kabir, Saleha, Peacock, Kelly, Pushparajah, Kuberan, Savis, Alex, Regan, Will, Pascall, Emma, Cleary, Aoife, Uy, Mirasol, Heard, Hannah, Carter, Michael, Tibby, Shane, Lillie, Jon, Riphagen, Shelley, MacDougall, Marilyn, Ben Griffths, Xabi Gomez, Waters, Gareth, Minen, Federico, Nyman, Andrew, Goulden, Miriam Fine, Sa, Mario, Lim, Ming, Bryne, Susan, Cadwgan, Jill, Lim, JP, Singh, Rahul, Tang, Shan, Lumsden, Dan, Senior, Sam, McMurtrie, Sarah, Norridge, Matthew, Emberson, Stephanie, Marr, Stacey, Felton, Victoria, Reid, Chris, Adalat, Shazia, Balasubramanian, Ramnath, Jones, Helen, Alamelu, Jay, Insua, Baba, Jeff, Jo Howard, Rees, David, Cheung, Moira, Santos, Rui, Jogeesvaran, Haran, Elbaaly, Heba, Reid, Catriona, Durve, Dipalee, Flohr, Carsten, Greenblatt, Danielle, Psomadakis, Cristina, Craythorne, Emma, Albert, Vanessa, Yardley, Iain, Brennan, Kirsty, Wolfe, Ingrid, Forman, Julia, Ben Baig, Deborah Woodman, Coniff, Harriet, Gordon, Anne, Taylor, Dan, Woude, Olga van der, McIntosh, Alysha

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IMPLICATIONS OF REVERTANT SOMATIC MOSAICISM IN BONE MARROW FAILURE SYNDROMES by Venugopal, Parvathy, Babic, Milena, Barnett, Christopher, Bray, Sarah, Brown, Anna, Cheah, Jesse, D'Andrea, Richard, Feng, Jinghua, Fine, Miriam, George, Amee, Guandalini, Michael, Hahn, Christopher, Hannan, Ross, Lawrence, David, Moore, Sarah, Philips, Kerry, Poplawski, Nicola, Saxon, Ben, Schreiber, Andreas, Scott, Hamish, Tirimacco, Amanda, To, Luen, Wilson, Peter, Yeoman, Alexandra, Young, Chun Chun

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Management of fluids in paediatric diabetic ketoacidosis: concerns over new guidance by Lillie, Jon, Boot, Elizabeth, Tibby, Shane M, McDougall, Marilyn, Nyman, Andrew, Griffiths, Benedict, Fine-Goulden, Miriam, Pavcnik, Maja, Annicq, Ariane, Riphagen, Shelley

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A multitiered analysis platform for genome sequencing: Design and initial findings of the Australian Genomics Cardiovascular Disorders Flagship by Austin, Rachel, Brown, Jaye S., Madelli, Evanthia O., Das, Debjani, Soka, Magdalena, Blue, Gillian M., Atherton, John J., Quinn, Michael C.J., Poplawski, Nicola K., Weintraub, Robert G., De Fazio, Paul, Thompson, Tina, Macciocca, Ivan, Ingles, Jodie, McGaughran, Julie, McLean, Alison, Smyth, Renee, Fatkin, Diane, McNamara, James, Medi, Caroline, Al-Shinnag, Mohammad, Metke, Alejandro, Sy, Raymond, Atherton, John J., Finlay, Keri, Milnes, Di, Austin, Rachel, Milward, Michael, Bagnall, Richard D., Giannoulatou, Eleni, Morrish, Ansley, Taylor, Shelby, Barnett, Chris, Blue, Gillian M., Mountain, Helen, Thompson, Tina, Bodek, Simon, Boggs, Kirsten, Ng, Chai-Ann, Trainer, Alison, Bogwitz, Michael, Haas, Mathilda, Trivedi, Gunjan, Boughtwood, Tiffany, Martinez, Noelia Nunez, Hayward, Janette, Vandenberg, Jamie, Brown, Jaye, Herrera, Carmen, Verma, Kunal, Richardson, Rob Bryson, Hill, Adam, Pachter, Nicholas, Vidgen, Miranda, Patel, Chirag, Vohra, Jitendra, Burns, Charlotte, Perrin, Mark, Cao, Michelle, Horton, Ari E., Perry, Matthew, Howting, Denise, Pflaumer, Andreas, Weintraub, Robert G., Ingles, Jodie, Phillips, Peta, Wilson, Meredith, Chalinor, Heather, Phuong, Thuan, Winlaw, David, Chang, Yuchen, Jackson, Matilda, Worgan, Lisa, Charitou, Theosodia, Jane-Pantaleo, Sarah, Chong, Belinda, Johnson, Renee, Quinn, Michael C.J., Collins, Felicity, Quinn, Michael, Rajagopalan, Sulekha, Cox, Kathy, Kummerfeld, Sarah, Das, Debjani, Davis, Jason, Rogers, Jonathan, Lunke, Sebastian, Sandaradura, Sarah, Dobbins, Julia, Mansour, Julia, Sherburn, Isabella, Dunwoodie, Sally L., Dwyer, Nathan, Mathew, Jacob, Singer, Emma, Elbracht-Leong, Stefanie, Mattiske, Tessa, Smerdon, Carla, Elliott, David, McGaughran, Julie

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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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Familial clustering of haematological malignancies: harbingers of wider germline cancer susceptibility by Scott, Hamish S., Brown, Anna L., Hiwase, Devendra, Schreiber, Andreas W., Feng, Jinghua, Babic, Milena, Poplawski, Nicola, Fine, Miriam, Rawlings, Lesley, Branford, Susan, Fuller, Stephen, Lewis, Ian, D’Andrea, Richard J., Hahn, Christopher N.

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Gaining clinical leadership experience through NHS England advisory support roles by Fine-Goulden, Miriam, Fielden, Jonathan

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Asthma in Pediatric Sickle Cell Acute Chest Syndrome: In An Inner City London Hospital by Bartram, Jack L, Fine-Goulden, Miriam R, Green, Dido, Ahmad, Rahail, Inusa, Baba PD

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