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    A Pan‐ E uropean Study of the C9orf72 Repeat Associated with FTLD : Geographic Prevalence, Genomic Instability, and Intermediate Repeats von van der Zee, Julie, Gijselinck, Ilse, Dillen, Lubina, Van Langenhove, Tim, Theuns, Jessie, Engelborghs, Sebastiaan, Philtjens, Stéphanie, Vandenbulcke, Mathieu, Sleegers, Kristel, Sieben, Anne, Bäumer, Veerle, Maes, Githa, Corsmit, Ellen, Borroni, Barbara, Padovani, Alessandro, Archetti, Silvana, Perneczky, Robert, Diehl‐Schmid, Janine, de Mendonça, Alexandre, Miltenberger‐Miltenyi, Gabriel, Pereira, Sónia, Pimentel, José, Nacmias, Benedetta, Bagnoli, Silvia, Sorbi, Sandro, Graff, Caroline, Chiang, Huei‐Hsin, Westerlund, Marie, Sanchez‐Valle, Raquel, Llado, Albert, Gelpi, Ellen, Santana, Isabel, Almeida, Maria Rosário, Santiago, Beatriz, Frisoni, Giovanni, Zanetti, Orazio, Bonvicini, Cristian, Synofzik, Matthis, Maetzler, Walter, vom Hagen, Jennifer Müller, Schöls, Ludger, Heneka, Michael T., Jessen, Frank, Matej, Radoslav, Parobkova, Eva, Kovacs, Gabor G., Ströbel, Thomas, Sarafov, Stayko, Tournev, Ivailo, Jordanova, Albena, Danek, Adrian, Arzberger, Thomas, Fabrizi, Gian Maria, Testi, Silvia, Salmon, Eric, Santens, Patrick, Martin, Jean‐Jacques, Cras, Patrick, Vandenberghe, Rik, De Deyn, Peter Paul, Cruts, Marc, Van Broeckhoven, Christine, van der Zee, Julie, Gijselinck, Ilse, Dillen, Lubina, Van Langenhove, Tim, Theuns, Jessie, Philtjens, Stéphanie, Sleegers, Kristel, Bäumer, Veerle, Maes, Githa, Corsmit, Ellen, Cruts, Marc, Van Broeckhoven, Christine, Engelborghs, Sebastiaan, De Deyn, Peter P., Cras, Patrick, Vandenbulcke, Mathieu, Borroni, Barbara, Padovani, Alessandro, Archetti, Silvana, Perneczky, Robert, Diehl‐Schmid, Janine, Synofzik, Matthis, Maetzler, Walter, Müller vom Hagen, Jennifer, Schöls, Ludger, Heneka, Michael T., Jessen, Frank, Ramirez, Alfredo, Kurzwelly, Delia, Sachtleben, Carmen, Mairer, Wolfgang, de Mendonça, Alexandre, Miltenberger‐Miltenyi, Gabriel, Pereira, Sónia, Firmo, Clara, Pimentel, José, Sanchez‐Valle, Raquel, Llado, Albert

    Veröffentlicht in Human mutation

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