Authors:
Granzow, M
Popp, S
Weber, S
Schoell, B
Holtgreve-Grez, H
Senf, L
Hager, D
Boschert, J
Scheurlen, W
Jauch, A
Citation: M. Granzow et al., Isochromosome 1q as an early genetic event in a child with intracranial ependymoma characterized by molecular cytogenetics, CANC GENET, 130(1), 2001, pp. 79-83
Authors:
Scholz, I
Popp, S
Granzow, M
Schoell, B
Holtgreve-Grez, H
Takeuchi, S
Schrappe, M
Harbott, J
Teigler-Schlegel, A
Zimmermann, M
Fischer, C
Koeffler, HP
Bartram, CR
Jauch, A
Citation: I. Scholz et al., Comparative genomic hybridization in childhood acute lymphoblastic leukemia: correlation with interphase cytogenetics and loss of heterozygosity analysis, CANC GENET, 124(2), 2001, pp. 89-97
Authors:
Granzow, M
Popp, S
Keller, M
Holtgreve-Grez, H
Brough, M
Schoell, B
Rauterberg-Ruland, I
Hager, HD
Tariverdian, G
Jauch, A
Citation: M. Granzow et al., Multiplex FISH telomere integrity assay identifies an unbalanced cryptic translocation der(5)t(3;5) (q27;p15.3) in a family with three mentally retarded individuals, HUM GENET, 107(1), 2000, pp. 51-57