Report of Jacobsen syndrome with a mild facial dysmorphism, severe hearing impairment and thrombocytopenia by Vaidas DIRSĖ, Loreta CIMBALISTIENĖ, Jūratė KASNAUSKIENĖ, Vaidutis KUČINSKAS

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Multiple Myeloma Immunophenotype Related to Chromosomal Abnormalities Used in Risk Assessment by Mantas Radzevičius, Vaidas Dirsė, Indrė Klimienė, Rėda Matuzevičienė, Zita Aušrelė Kučinskienė, Valdas Pečeliūnas

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A De Novo 8q22.2q22.3 Interstitial Microdeletion in a Girl with Developmental Delay and Congenital Defects by Ruta Kalinauskiene, Deimante Brazdziunaite, Neringa Burokiene, Vaidas Dirsė, Ausra Morkuniene, Algirdas Utkus, Egle Preiksaitiene

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Case Report: Specific ABL-Inhibitor Imatinib Is an Effective Targeted Agent as the First Line Therapy to Treat B-Cell Acute Lymphoblastic Leukemia With a Cryptic NUP214::ABL1 Gene... by Egle Stukaite-Ruibiene, Rimvydas Norvilas, Rimvydas Norvilas, Vaidas Dirse, Sigita Stankeviciene, Goda Elizabeta Vaitkeviciene, Goda Elizabeta Vaitkeviciene

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Genetic Subtypes and Outcome of Patients Aged 1 to 45 Years Old With Acute Lymphoblastic Leukemia in the NOPHO ALL2008 Trial by Ulrika Norén-Nyström, Mette K. Andersen, Gisela Barbany, Vaidas Dirse, Martine Eilert-Olsen, Marie Engvall, Arja Harila-Saari, Mats Heyman, Randi Hovland, Satu Häikiö, Jón J. Jónsson, Ritva Karhu, Eigil Kjeldsen, Anna Norberg, Birgitte S. Preiss, Kati Pulkkinen, Petter Quist-Paulsen, Hannele Räsänen, Kjeld Schmiegelow, Anne Seitsonen, Helene Sjögren, Pille Tammur, Bertil Johansson

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