Authors:
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Marg, W
Mergenthaler, S
Eggermann, K
Schemmel, V
Stoffers, U
Zerres, K
Spranger, S
Citation: T. Eggermann et al., Origin of uniparental disomy 6: presentation of a new case and review on the literature, ANN GENET, 44(1), 2001, pp. 41-45
Authors:
Bohlander, SK
Muschinsky, V
Schrader, K
Siebert, R
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Harder, L
Schemmel, V
Fonatsch, C
Ludwig, WD
Hiddemann, W
Dreyling, MH
Citation: Sk. Bohlander et al., Molecular analysis of the CALM/AF10 fusion: identical rearrangements in acute myeloid leukemia, acute lymphoblastic leukemia and malignant lymphoma patients, LEUKEMIA, 14(1), 2000, pp. 93-99
Authors:
Stanulla, M
Stumm, M
Dieckvoss, BO
Seidemann, K
Schemmel, V
Brechlin, AM
Schrappe, M
Welte, K
Reiter, A
Citation: M. Stanulla et al., No evidence for a major role of heterozygous deletion 657del5 within the NBS1 gene in the pathogenesis of non-Hodgkin's lymphoma of childhood and adolescence, BR J HAEM, 109(1), 2000, pp. 117-120
Authors:
Valent, P
Escribano, L
Parwaresch, RM
Schemmel, V
Schwartz, LB
Sotlar, K
Sperr, WR
Horny, HP
Citation: P. Valent et al., Recent advances in mastocytosis research - Summary of the Vienna Mastocytosis Meeting 1998, INT A AL IM, 120(1), 1999, pp. 1-7
Authors:
Siebert, R
Gesk, S
Harder, L
Steinemann, D
Grote, W
Schlegelberger, B
Tiemann, M
Wlodarska, I
Schemmel, V
Citation: R. Siebert et al., Complex variant translocation t(1;2) with TPM3-ALK fusion due to cryptic ALK gene rearrangement in anaplastic large-cell lymphoma, BLOOD, 94(10), 1999, pp. 3614-3617