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    Detection of clinically relevant variants in the TP53 gene below 10% allelic frequency: A multicenter study by ERIC, the European Research Initiative on CLL von Pavlova, Sarka, Malcikova, Jitka, Radova, Lenka, Bonfiglio, Silvia, Cowland, Jack B., Brieghel, Christian, Andersen, Mette K., Karypidou, Maria, Biderman, Bella, Doubek, Michael, Lazarian, Gregory, Rapado, Inmaculada, Vynck, Matthijs, Porret, Naomi A., Andres, Martin, Rosenberg, Dina, Sahar, Dvora, Martínez‐Laperche, Carolina, Buño, Ismael, Hindley, Andrew, Donaldson, David, Sánchez, Julio B., García‐Marco, José A., Serrano‐Alcalá, Alicia, Ferrer‐Lores, Blanca, Fernández‐Rodriguez, Concepción, Bellosillo, Beatriz, Stilgenbauer, Stephan, Tausch, Eugen, Nikdin, Hero, Quinn, Fiona, Atkinson, Emer, van de Corput, Lisette, Yildiz, Cafer, Bilbao‐Sieyro, Cristina, Florido, Yanira, Thiede, Christian, Schuster, Caroline, Stoj, Anastazja, Czekalska, Sylwia, Chatzidimitriou, Anastasia, Laidou, Stamatia, Bidet, Audrey, Dussiau, Charles, Nollet, Friedel, Piras, Giovanna, Monne, Maria, Smirnova, Svetlana, Nikitin, Eugene, Sloma, Ivan, Claudel, Alexis, Largeaud, Laetitia, Ysebaert, Loïc, Valk, Peter J. M., Christian, Amy, Walewska, Renata, Oscier, David, Sebastião, Marta, da Silva, Maria Gomes, Galieni, Piero, Angelini, Mario, Rossi, Davide, Spina, Valeria, Matos, Sónia, Martins, Vânia, Stokłosa, Tomasz, Pepek, Monika, Baliakas, Panagiotis, Andreu, Rafa, Luna, Irene, Kahre, Tiina, Murumets, Ülle, Pikousova, Tereza, Kurucova, Terezia, Laird, Sophie, Ward, Daniel, Alcoceba, Miguel, Balanzategui, Ana, Scarfo, Lydia, Gandini, Francesca, Zapparoli, Ettore, Blanco, Adoración, Abrisqueta, Pau, Rodríguez‐Vicente, Ana E., Benito, Rocío, Bravetti, Clotilde, Davi, Frédéric, Gameiro, Paula, Martinez‐Lopez, Joaquin, Tazón‐Vega, Bárbara, Baran‐Marszak, Fanny, Davis, Zadie, Catherwood, Mark, Sudarikov, Andrey, Rosenquist, Richard, Niemann, Carsten U., Stamatopoulos, Kostas, Ghia, Paolo, Pospisilova, Sarka

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