Mitotic recombination and compound-heterozygous mutations are predominant NF1-inactivating mechanisms in children with juvenile myelomonocytic leukemia and neurofibromatosis type 1 von STEINEMANN, Doris, ARNING, Larissa, PRAULICH, Inka, STUHRMANN, Manfred, HASLE, Henrik, STARY, Jan, SCHLEGELBERGER, Brigitte, NIEMEYER, Charlotte M, FLOTHO, Christian

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Clonal heterogeneity in childhood myelodysplastic syndromes-Challenge for the detection of chromosomal imbalances by array-CGH von Praulich, Inka, Tauscher, Marcel, Göhring, Gudrun, Glaser, Stefanie, Hofmann, Winfried, Feurstein, Simone, Flotho, Christian, Lichter, Peter, Niemeyer, Charlotte M., Schlegelberger, Brigitte, Steinemann, Doris

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Mutations in the let-7 binding site - a mechanism of RAS activation in juvenile myelomonocytic leukemia? von STEINEMANN, Doris, TAUSCHER, Marcel, PRAULICH, Inka, NIEMEYER, Charlotte M, FLOTHO, Christian, SCHLEGELBERGER, Brigitte

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A rare case of t(11;22) in a mantle cell lymphoma like B-cell neoplasia resulting in a fusion of IGL and CCND1: case report von Rocha, Cristiano Krings, Praulich, Inka, Gehrke, Iris, Hallek, Michael, Kreuzer, Karl-Anton

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Phenotypic spectrum of BLM‐ and RMI1‐related Bloom syndrome von Gönenc, Ipek Ilgin, Elcioglu, Nursel H., Martinez Grijalva, Carolina, Aras, Seda, Großmann, Nadine, Praulich, Inka, Altmüller, Janine, Kaulfuß, Silke, Li, Yun, Nürnberg, Peter, Burfeind, Peter, Yigit, Gökhan, Wollnik, Bernd

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Patient-specific analysis of FLT3 internal tandem duplications for the prognostication and monitoring of acute myeloid leukemia von Schiller, Joanna, Praulich, Inka, Krings Rocha, Cristiano, Kreuzer, Karl-Anton

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Highly Sensitive Monitoring of Minimal Residual Disease in FLT3-itd-Positive Acute Myeloid Leukemia Patients with a Mutation Specific Quantitative-PCR Method von Schiller, Joanna, Praulich, Inka, Hallek, Michael, Kreuzer, Karl-Anton

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Constitutional trisomy 8p11.21‐q11.21 mosaicism: a germline alteration predisposing to myeloid leukaemia von Ripperger, Tim, Tauscher, Marcel, Praulich, Inka, Pabst, Brigitte, Teigler‐Schlegel, Andrea, Yeoh, Allen, Göhring, Gudrun, Schlegelberger, Brigitte, Flotho, Christian, Niemeyer, Charlotte M., Steinemann, Doris

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Patient‐specific analysis of FLT 3 internal tandem duplications for the prognostication and monitoring of acute myeloid leukemia von Schiller, Joanna, Praulich, Inka, Krings Rocha, Cristiano, Kreuzer, Karl‐Anton

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Array-CGH in Childhood MDS von Tauscher, Marcel, Praulich, Inka, Steinemann, Doris

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Gain of the Centromeric Region of Chromosome 8, a New Germline Alteration In Juvenile Myelomonocytic Leukemia von Steinemann, Doris, Ripperger, Tim, Tauscher, Marcel, Praulich, Inka, Göhring, Gudrun, Pabst, Brigitte, Teigler-Schlegel, Andrea, Schlegelberger, Brigitte, Niemeyer, Charlotte M, Flotho, Christian

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Protein microarrays: Reduced autofluorescence and improved LOD von Walter, Johanna-Gabriela, Stahl, Frank, Reck, Michael, Praulich, Inka, Nataf, Yakir, Hollas, Markus, Pflanz, Karl, Melzner, Dieter, Shoham, Yuval, Scheper, Thomas

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Mutation analysis of the HAX1 gene in childhood myelodysplastic syndrome von Steinemann, Doris, Praulich, Inka, Otto, Noreen, Göhring, Gudrun, Niemeyer, Charlotte M., Schlegelberger, Brigitte

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Molecular characterization of the rare translocation t(3;10)(q26;q21) in an acute myeloid leukemia patient von Jancuskova, Tereza, Plachy, Radek, Zemankova, Lucie, Hardekopf, David Warren, Stika, Jiri, Zejskova, Lenka, Praulich, Inka, Kreuzer, Karl-Anton, Rothe, Achim, Othman, Moneeb Ak, Kosyakova, Nadezda, Pekova, Sona

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New 3D black substrate for protein microarrays with improved dynamic range von Hollas, Markus, Jallerat, Eric, Pflanz, Karl, Praulich, Inka, Walter, Johanna, Stahl, Frank, Scheper, Thomas

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Molecular characterization of the rare translocation t(3;10)(q26;q21) in an acute myeloid leukemia patient von Jancuskova, Tereza, Plachy, Radek, Zemankova, Lucie, Hardekopf, David Warren, Stika, Jiri, Zejskova, Lenka, Praulich, Inka, Kreuzer, Karl-Anton, Rothe, Achim, Othman, Moneeb Ak, Kosyakova, Nadezda, Pekova, Sona

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