Treffer 1 - 20 von 288 für Suche 'ZWOLINSKI, M. D', Suchdauer: 1,40s Treffer weiter einschränken
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    Widening of the genetic and clinical spectrum of Lamb–Shaffer syndrome, a neurodevelopmental disorder due to SOX5 haploinsufficiency von Zawerton, Ash, Mignot, Cyril, Sigafoos, Ashley, Blackburn, Patrick R., Haseeb, Abdul, McWalter, Kirsty, Ichikawa, Shoji, Nava, Caroline, Keren, Boris, Charles, Perrine, Marey, Isabelle, Tabet, Anne-Claude, Levy, Jonathan, Perrin, Laurence, Hartmann, Andreas, Lesca, Gaetan, Schluth-Bolard, Caroline, Monin, Pauline, Dupuis-Girod, Sophie, Guillen Sacoto, Maria J., Schnur, Rhonda E., Zhu, Zehua, Poisson, Alice, El Chehadeh, Salima, Alembik, Yves, Bruel, Ange-Line, Lehalle, Daphné, Nambot, Sophie, Moutton, Sébastien, Odent, Sylvie, Jaillard, Sylvie, Dubourg, Christèle, Hilhorst-Hofstee, Yvonne, Barbaro-Dieber, Tina, Ortega, Lucia, Bhoj, Elizabeth J., Masser-Frye, Diane, Bird, Lynne M., Lindstrom, Kristin, Ramsey, Keri M., Narayanan, Vinodh, Fassi, Emily, Willing, Marcia, Cole, Trevor, Salter, Claire G., Akilapa, Rhoda, Vandersteen, Anthony, Canham, Natalie, Rump, Patrick, Gerkes, Erica H., Klein Wassink-Ruiter, Jolien S., Bijlsma, Emilia, Hoffer, Mariëtte, Vargas, Marcelo, Wojcik, Antonina, Cherik, Florian, Francannet, Christine, Rosenfeld, Jill A., Machol, Keren, Scott, Daryl A., Bacino, Carlos A., Wang, Xia, Clark, Gary D., Bertoli, Marta, Zwolinski, Simon, Thomas, Rhys H., Akay, Ela, Chang, Richard C., Bressi, Rebekah, Sanchez Russo, Rossana, Srour, Myriam, Russell, Laura, Goyette, Anne-Marie E., Dupuis, Lucie, Mendoza-Londono, Roberto, Karimov, Catherine, Joseph, Maries, Nizon, Mathilde, Cogné, Benjamin, Kuechler, Alma, Piton, Amélie, Klee, Eric W., Lefebvre, Véronique, Clark, Karl J., Depienne, Christel

    Veröffentlicht in Genetics in medicine

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    Long-course oxaliplatin-based preoperative chemoradiation versus 5 × 5 Gy and consolidation chemotherapy for cT4 or fixed cT3 rectal cancer: results of a randomized phase III study... von Bujko, K., Wyrwicz, L., Rutkowski, A., Malinowska, M., Pietrzak, L., Kryński, J., Olędzki, J., Kuśnierz, J., Zając, L., Szczepkowski, M., Tarnowski, W., Kosakowska, E., Zwoliński, J., Winiarek, M., Bęczkowska, K., Polkowski, W., Styliński, R., Wierzbicki, R., Bury, P., Jankiewicz, M., Paprota, K., Lewicka, M., Ciseł, B., Skórzewska, M., Maciejczyk, A., Kapturkiewicz, B., Dybko, A., Hajac, Ł., Leśniak, T., Zygulska, J., Jantner, D., Chudyba, E., Las-Jankowska, M., Jankowski, M., Kołodziejski, L., Żelazowska-Omiotek, U., Kępka, L., Kolb-Sielecki, J., Toczko, Z., Fedorowicz, Z., Dziki, A., Nawrocki, G., Sopyło, R., Markiewicz, W., Kędzierawski, P., Wydmański, J., Albiński, J., Banaś, R., Chmielowska, E., Bal, W., Baszczyk-Mnich, J., Bialas, M., Borowiec, T., Cencelewicz, A., Chomik, K., Chwaliński, M., Ciepela, I., Florek, A., Górnicki, A., Jeziorski, K., Józwicki, W., Kobiela, J., Koda, M., Kołodziej, P., Kruszewski, P., Kryj, M., Kuciel-Lisiecka, G., Kwiatkowski, R., Lachowski, A., Liszka-Dalecki, P., Majewski, A., Majewski, W., Majsak, T., Maka, D., Malka, M., Mazurkiewicz, A., Morawiec, J., Nogal, E., Olejniczak, M., Olkowski, D., Ostrowska-Cichocka, K., Pietruszka, M., Piotrkowski, G., Plewicka, M., Porzuczek-Zuziak, D., Reszke, J., Rychter, A., Sadowski, J., Serkies, K., Srutek, E., Szóstak, B., Tuziak, T., Tyralik, D., Skoczylas, J., Wachua, E., Wandzel, P., Winkler-Spytkowska, B., Wojtasik, P., Wroński, K., Zygulski, I.

    Veröffentlicht in Annals of oncology

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    Widening of the genetic and clinical spectrum of Lamb–Shaffersyndrome, a neurodevelopmental disorder due to SOX5haploinsufficiency von Ash, Zawerton, Mignot Cyril, Sigafoos Ashley, Blackburn, Patrick R, Haseeb Abdul, McWalter Kirsty, Ichikawa Shoji, Nava, Caroline, Keren, Boris, Perrine, Charles, Marey Isabelle, Tabet Anne-Claude, Levy, Jonathan, Perrin, Laurence, Hartmann, Andreas, Lesca Gaetan, Schluth-Bolard Caroline, Monin, Pauline, Dupuis-Girod, Sophie, Guillen Sacoto Maria J, Schnur, Rhonda E, Zhu Zehua, Poisson, Alice, Salima, El Chehadeh, Alembik Yves, Ange-Line, Bruel, Lehalle Daphné, Nambot Sophie, Moutton Sébastien, Odent Sylvie, Jaillard Sylvie, Dubourg Christèle, Hilhorst-Hofstee Yvonne, Barbaro-Dieber Tina, Ortega, Lucia, Bhoj, Elizabeth J, Masser-Frye, Diane, Bird, Lynne M, Lindstrom, Kristin, Ramsey, Keri M, Narayanan Vinodh, Fassi, Emily, Willing, Marcia, Cole, Trevor, Salter, Claire G, Akilapa Rhoda, Vandersteen, Anthony, Canham, Natalie, Rump, Patrick, Gerkes, Erica H, Klein Wassink-Ruiter Jolien S, Bijlsma Emilia, Hoffer, Mariëtte J, Vargas, Marcelo, Wojcik Antonina, Cherik Florian, Francannet Christine, Rosenfeld, Jill A, Machol Keren, Scott, Daryl A, Bacino, Carlos A, Wang, Xia, Clark, Gary D, Bertoli, Marta, Zwolinski, Simon, Thomas, Rhys H, Akay Ela, Chang, Richard C, Bressi Rebekah, Sanchez Russo Rossana, Srour Myriam, Russell, Laura, Goyette, Anne-Marie E, Dupuis Lucie, Mendoza-Londono, Roberto, Karimov, Catherine, Maries, Joseph, Nizon Mathilde, Cogné Benjamin, Kuechler Alma, Piton Amélie, Klee, Eric W, Lefebvre Véronique, Clark, Karl J, Depienne Christel

    Veröffentlicht in Genetics in medicine

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