Browsing by Author Legius, Eric

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Showing results 1 to 4 of 4
Issue DateTitleAuthor(s)
1-Feb-2023Deep genomic analysis of malignant peripheral nerve sheath tumor cell lines challenges current malignant peripheral nerve sheath tumor diagnosisMagallón Lorenz, Miriam; Terribas, Ernest; Ortega Bertran, Sara; Creus Bachiller, Edgar; Fernández, Marco; Requena, Gerard; Rosas, Inma; Mazuelas, Helena; Uriarte Arrazola, Itziar; Negro, Alex; Lausová, Tereza; Castellanos, Elisabeth; Blanco, Ignacio; Devries, George; Kawashima, Hiroyuki; Legius, Eric; Brems, Hilde; Mautner, Viktor; Kluwe, Lan; Ratner, Nancy; Wallace, Margaret; Fernández-Rodríguez, Juana; Lázaro García, Conxi; Fletcher, Jonathan A.; Reuss, David; Carrió, Meritxell; Gel, Bernat; Serra Arenas, Eduard
1-Dec-2022Genotype-phenotype associations in a large PTEN Hamartoma Tumor Syndrome (PHTS) patient cohortHendricks, Linda A.J.; Hoogerbrugge, Nicoline; Venselaar, Hanka; Aretz, Stefan; Spier, Isabel; Legius, Eric; Brems, Hilde; De Putter, Robin; Claes, Kathleen B.M.; Evans, D. Gareth; Woodward, Emma R.; Genuardi, Maurizio; Brugnoletti, Fulvia; Van Ierland, Yvette; Dijke, Kim; Tham, Emma; Tesi, Bianca; Schuurs Hoeijmakers, Janneke H.M.; Branchaud, Maud; Salvador, Hector; Jahn, Arne; Schnaiter, Simon; Anastasiadou, Violetta Christophidou; Brunet, Joan; Oliveira, Carla; Roht, Laura; Blatnik, Ana; Irmejs, Arvids; Mensenkamp, Arjen R.; Vos, Janet R.; Duijkers, Floor; Giltay, Jacques C.; Van Hest, Liselotte P.; Kleefstra, Tjitske; Leter, Edward M.; Nielsen, Maartje; Nijmeijer, Sebastiaan W.R.; Olderode-berends, Maran J.W.
Feb-2020Mutational spectrum by phenotype: panel-based NGS testing of patients with clinical suspition of RASopathy and children with multiple café-au-lait maculesCastellanos, Elisabeth; Rosas, Inma; Negro, Alex; Gel Moreno, Bernat; Alibés, Andreu; Baena, Neus; Pineda Marfà, Mercè; Pi, Graciela; Pintos, Guillem; Salvador, Hector; Lázaro García, Conxi; Blanco Guillermo, Ignacio; Vilageliu i Arqués, Lluïsa; Brems, Hilde; Grinberg Vaisman, Daniel Raúl; Legius, Eric; Serra Arenas, Eduard
2-Jun-2014SVA retrotransposon insertion-associated deletion represents a novel mutational mechanism underlying large genomic copy number changes with non-recurrent breakpointsVogt, Julia; Bengesser, Kathrin; Claes, Kathleen B. M.; Wimmer, Katharina; Mautner, Victor-Felix; van Minkelen, Rick; Legius, Eric; Brems, Hilde; Upadhyaya, Meena; Högel, Josef; Lázaro García, Conxi; Rosenbaum, Thorsten; Bammert, Simone; Messiaen, Ludwine M.; Cooper, David N.; Kehrer-Sawatzki, Hildegard