Search Results - Hollingsworth, Laura K

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    High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies by Myers, Candace T., Cossette, Patrick, Lemay, Philippe, Spiegelman, Dan, Laporte, Alexandre Dionne, Nassif, Christina, Diallo, Ousmane, Monlong, Jean, Cadieux-Dion, Maxime, Dobrzeniecka, Sylvia, Meloche, Caroline, Retterer, Kyle, Cho, Megan T., Rosenfeld, Jill A., Bi, Weimin, Massicotte, Christine, Miguet, Marguerite, Brunga, Ledia, Regan, Brigid M., Mo, Kelly, Tam, Cory, Hollingsworth, Georgie, FitzPatrick, David R., Canham, Natalie, Blair, Edward, Kerr, Bronwyn, Fry, Andrew E., Thomas, Rhys H., Shelagh, Joss, Hurst, Jane A., Brittain, Helen, Blyth, Moira, Lebel, Robert Roger, Gerkes, Erica H., Davis-Keppen, Laura, Stein, Quinn, Dorison, Sara J., Benke, Paul J., Fassi, Emily, Corsten-Janssen, Nicole, Kamsteeg, Erik-Jan, Mau-Them, Frederic T., Bruel, Ange-Line, Verloes, Alain, Õunap, Katrin, Wojcik, Monica H., Albert, Dara V.F., Venkateswaran, Sunita, Ware, Tyson, Liu, Yu-Chi, Mohammad, Shekeeb S., Bizargity, Peyman, Bacino, Carlos A., Leuzzi, Vincenzo, Martinelli, Simone, Dallapiccola, Bruno, Tartaglia, Marco, Blumkin, Lubov, Wierenga, Klaas J., Purcarin, Gabriela, O’Byrne, James J., Stockler, Sylvia, Lehman, Anna, Keren, Boris, Nougues, Marie-Christine, Mignot, Cyril, Auvin, Stéphane, Nava, Caroline, Hiatt, Susan M., Bebin, Martina, Shao, Yunru, Scaglia, Fernando, Frye, Richard E., Jarjour, Imad T., Jacques, Stéphanie, Boucher, Renee-Myriam, Riou, Emilie, Srour, Myriam, Carmant, Lionel, Lortie, Anne, Major, Philippe, Diadori, Paola, Dubeau, François, D’Anjou, Guy, Bourque, Guillaume, Berkovic, Samuel F., Sadleir, Lynette G., Campeau, Philippe M., Kibar, Zoha, Lafrenière, Ronald G., Girard, Simon L., Mercimek-Mahmutoglu, Saadet, Boelman, Cyrus, Rouleau, Guy A., Scheffer, Ingrid E., Mefford, Heather C., Andrade, Danielle M., Rossignol, Elsa, Minassian, Berge A., Michaud, Jacques L.

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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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