Folyóiratcikkek tallózása szerző szerint "Piko, Henriett"

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  • Complex X chromosome rearrangement associated with multiorgan autoimmunity 
    Haltrich, Irén; Piko, Henriett; Pamjav H; Somogyi, Anikó; Volgyi A; David D; Beke, Artúr; Garamvölgyi, Zoltán; Kiss, Eszter; Karcagi V; Fekete, György (2015)
    BACKGROUND: Turner syndrome, a congenital condition that affects 1/2,500 births, results from absence or structural alteration of the second sex chromosome. Turner syndrome is usually associated with short stature, gonadal ...
  • Validation of the United Kingdom copy-number alteration classifier in 3239 children with B-cell precursor ALL 
    Hamadeh, Lina; Enshaei, Amir; Schwab, Claire; Alonso, Cristina N; Attarbaschi, Andishe; Barbany, Gisela; den Boer, Monique L; Boer, Judith M; Braun, Marcin; Dalla Pozza, Luciano; Elitzur, Sarah; Emerenciano, Mariana; Fechina, Larisa; Felice, Maria Sara; Fronkova, Eva; Haltrich, Irén; Heyman, Mats M; Horibe, Keizo; Imamura, Toshihiko; Jeison, Marta; Kovács, Gábor; Kuiper, Roland P; Mlynarski, Wojciech; Nebral, Karin; Ivanov Öfverholm, Ingegerd; Pastorczak, Agata; Pieters, Rob; Piko, Henriett; Pombo-de-Oliveira, Maria S; Rubio, Patricia; Strehl, Sabine; Stary, Jan; Sutton, Rosemary; Trka, Jan; Tsaur, Grigory; Venn, Nicola; Vora, Ajay; Yano, Mio; Harrison, Christine J; Moorman, Anthony V (2019)
    Genetic abnormalities provide vital diagnostic and prognostic information in pediatric acute lymphoblastic leukemia (ALL) and are increasingly used to assign patients to risk groups. We recently proposed a novel classifier ...