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NEXT GENERATION SEQUENCING APPROACH TO BONE MARROW FAILURE SYNDROMES – PORTUGUESE EXPERIENCE by Margarida Coucelo, Joana Azevedo, Isabel Bogalho, Ana Teresa Simões, Ana Catarina Oliveira, Sara Batalha, Conceição Constanço, Teresa Melo, José Carlos Almeida, Joana Desterro, Patricia Ribeiro, Emilia Costa, Anabela Ferrão, Paula Kjollerstrom, Catarina Geraldes

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GENOTYPE/PHENOTYPE ASSOCIATIONS IN 174 INDIVIDUALS WITH GERMLINE GATA2 MUTATIONS by Lili Kotmayer, Emilia Kozyra, Maximilian Kaiser, Michael Dworzak, Barbara De Moerloose, Jan Starý, Henrik Hasle, Kirsi Jahnukainen, Sophia Polychronopoulou, Krisztián Kállay, Owen Smith, Shlomit Barzilai, Riccardo Masetti, Jochen Buechner, Marek Ussowicz, Paula Kjollerstrom, Ivana Boďová, Marko Kavcic, Albert Catala, Dominik Turkiewicz, Markus Schmugge, Valérie De Haas, Rebecca Voss, Anna Bigas, Damia Romero, Csaba Bödör, Miriam Erlacher, Alessandra Giorgetti, Charlotte Niemeyer, Marcin Wlodarski

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NPM1 MUTATIONS IN CHILDREN WITH MYELODYSPLASTIC SYNDROME WITH EXCESS BLASTS by Ayami Yoshimi, Miriam Erlacher, Peter Noellke, Senthilkumar Ramamoorthy, Gudrun Göhring, Shlomit Barzilai – Birenboim, Ivana Bodova, Jochen Buechner, Albert Catala, Valérie De Haas, Barbara De Moerloose, Michael Dworzak, Henrik Hasle, Kirsi Jahnukainen, Krisztian Kallay, Marko Kavcic, Paula Kjollerstrom, Franco Locatelli, Riccardo Masetti, Sophia Polychronopoulou, Markus Schmugge, Owen Smith, Jan Stary, Dominik Turkiewicz, Marek Ussowicz, Natalia Rotari, Marcin Wlodarski, Brigitte Strahm, Charlotte Niemeyer

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