Electronic checklist command sequencer von Snider, Ernest A, Zellmer, Justin T, Sisson, James E, Gray, Christel P, Kanne, Bryon S, Barber, Sarah

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ELECTRONIC CHECKLIST COMMAND SEQUENCER von Snider, Ernest A, Zellmer, Justin T, Sisson, James E, Gray, Christel P, Kanne, Bryon S, Barber, Sarah

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ELECTRONIC CHECKLIST COMMAND SEQUENCER von BARBER, Sarah, ZELLMER, Justin T, KANNE, Bryon S, SISSON, James E, SNIDER, Ernest A, GRAY, Christel P

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The evolution of the DLK1-DIO3 imprinted domain in mammals von Edwards, Carol A, Mungall, Andrew J, Matthews, Lucy, Ryder, Edward, Gray, Dionne J, Pask, Andrew J, Shaw, Geoffrey, Graves, Jennifer A M, Rogers, Jane, Dunham, Ian, Renfree, Marilyn B, Ferguson-Smith, Anne C

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Genomic Aberrations and Late Recurrence in Postmenopausal Women with Hormone Receptor-positive Early Breast Cancer: Results from the SOLE Trial von Guerini-Rocco, Elena, Gray, Kathryn P, Fumagalli, Caterina, Reforgiato, Marta Rita, Leone, Isabella, Rafaniello Raviele, Paola, Munzone, Elisabetta, Kammler, Roswitha, Neven, Patrick, Hitre, Erika, Jerusalem, Guy, Simoncini, Edda, Gombos, Andrea, Deleu, Ines, Karlsson, Per, Aebi, Stefan, Chirgwin, Jacquie, Di Lauro, Vincenzo, Thompson, Alastair, Graas, Marie-Pascale, Barber, Matthew, Fontaine, Christel, Loibl, Sibylle, Gavilá, Joaquín, Kuroi, Katsumasa, Müller, Bettina, O'Reilly, Seamus, Di Leo, Angelo, Goldhirsch, Aron, Viale, Giuseppe, Barberis, Massimo, Regan, Meredith M, Colleoni, Marco

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Genomic Aberrations and Late Recurrence in Postmenopausal Women with Hormone Receptor-positive Early Breast Cancer: Results from the SOLE Trial von Guerini-Rocco, Elena, Gray, Kathryn P, Fumagalli, Caterina, Reforgiato, Marta Rita, Leone, Isabella, Raviele, Paola Rafaniello, Munzone, Elisabetta, Kammler, Roswitha, Neven, Patrick, Hitre, Erika, Jerusalem, Guy, Simoncini, Edda, Gombos, Andrea, Deleu, Ines, Karlsson, Per, Aebi, Stefan, Chirgwin, Jacquie, Di Lauro, Vincenzo, Thompson, Alastair, Graas, Marie-Pascale, Barber, Matthew, Fontaine, Christel, Loibl, Sibylle, Gavila, Joaquin, Kuroi, Katsumasa, Muller, Bettina, O'Reilly, Seamus, Di Leo, Angelo, Goldhirsch, Aron, Viale, Giuseppe, Barberis, Massimo, Regan, Meredith M, Colleoni, Marco

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Genomic and phenotypic characterization of 404 individuals with neurodevelopmental disorders caused by CTNNB1 variants von Kayumi, Sayaka, Pérez-Jurado, Luis A, Palomares, María, Rangu, Sneha, Sheppard, Sarah E, Chung, Wendy K, Kruer, Michael C, Kharbanda, Mira, Amor, David J, McGillivray, George, Cohen, Julie S, García-Miñaúr, Sixto, van Eyk, Clare L, Harper, Kelly, Jolly, Lachlan A, Webber, Dani L, Barnett, Christopher P, Santos-Simarro, Fernando, Pacio-Míguez, Marta, Pozo, Angela Del, Bakhtiari, Somayeh, Deardorff, Matthew, Dubbs, Holly A, Izumi, Kosuke, Grand, Katheryn, Gray, Christopher, Mark, Paul R, Bhoj, Elizabeth J, Li, Dong, Ortiz-Gonzalez, Xilma R, Keena, Beth, Zackai, Elaine H, Goldberg, Ethan M, Perez de Nanclares, Guiomar, Pereda, Arrate, Llano-Rivas, Isabel, Arroyo, Ignacio, Fernández-Cuesta, María Ángeles, Thauvin-Robinet, Christel, Faivre, Laurence, Garde, Aurore, Mazel, Benoit, Bruel, Ange-Line, Tress, Michael L, Brilstra, Eva, Fine, Amena Smith, Crompton, Kylie E, Stegmann, Alexander P A, Sinnema, Margje, Stevens, Servi C J, Nicolai, Joost, Lesca, Gaetan, Lion-François, Laurence, Haye, Damien, Chatron, Nicolas, Piton, Amelie, Nizon, Mathilde, Cogne, Benjamin, Srivastava, Siddharth, Bassetti, Jennifer, Muss, Candace, Gripp, Karen W, Procopio, Rebecca A, Millan, Francisca, Morrow, Michelle M, Assaf, Melissa, Moreno-De-Luca, Andres, Joss, Shelagh, Hamilton, Mark J, Bertoli, Marta, Foulds, Nicola, McKee, Shane, MacLennan, Alastair H, Gecz, Jozef, Corbett, Mark A

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