Search Results - Ritterbach, Jutta

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  1. 1
    Trisomy 21 is a recurrent secondary aberration in childhood acute lymphoblastic leukemia with TEL/AML1 gene fusion

    Trisomy 21 is a recurrent secondary aberration in childhood acute lymphoblastic leukemia with TEL/AML1 gene fusion by Loncarevic, Ivan F., Roitzheim, Barbara, Ritterbach, Jutta, Viehmann, Susanne, Borkhardt, Arndt, Lampert, Fritz, Harbott, Jochen

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    Trisomy 21 is a recurrent secondary aberration in childhood acute lymphoblastic leukemia withTEL/AML1 gene fusion

    Trisomy 21 is a recurrent secondary aberration in childhood acute lymphoblastic leukemia withTEL/AML1 gene fusion by Loncarevic, Ivan F., Roitzheim, Barbara, Ritterbach, Jutta, Viehmann, Susanne, Borkhardt, Arndt, Lampert, Fritz, Harbott, Jochen

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  3. 3
    Characterization of chromosome 8 abnormalities by fluorescence in situ hybridization in childhood B-acute lymphoblastic leukemia/non-Hodgkin lymphoma

    Characterization of chromosome 8 abnormalities by fluorescence in situ hybridization in childhood B-acute lymphoblastic leukemia/non-Hodgkin lymphoma by Nishida, Kazuhiro, Ritterbach, Jutta, Repp, Reinald, Harbott, Jochen, Lampert, Fritz

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    12q13, A new recurrent breakpoint in acute non-lymphoblastic leukemia

    12q13, A new recurrent breakpoint in acute non-lymphoblastic leukemia by Seyger, Marieke M.B., Ritterbach, Jutta, Creutzig, Ursula, Gnekow, Astrid K., Göbel, Ulrich, Graf, Norbert, Reiter, Alfred, Lampert, Fritz, Harbott, Jochen

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