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Results:
1-14
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Results: 14
Authors:
Scheil, S
Bruderlein, S
Liehr, T
Starke, H
Herms, J
Schulte, M
Moller, P
Citation: S. Scheil et al., Genome-wide analysis of sixteen chordomas by comparative genomic hybridization and cytogenetics of the first human chordoma cell line, U-CHI, GENE CHROM, 32(3), 2001, pp. 203-211
Authors:
Dufke, A
Walczak, C
Liehr, T
Starke, H
Trifonov, V
Rubtsov, N
Schoning, M
Enders, H
Eggermann, T
Citation: A. Dufke et al., Partial tetrasomy 12pter-12p12.3 in a girl with Pallister-Killian syndrome: extraordinary finding of an analphoid, inverted duplicated marker, EUR J HUM G, 9(8), 2001, pp. 572-576
Authors:
Rump, A
Kasper, G
Hayes, C
Wen, GP
Starke, H
Liehr, T
Lehmann, R
Lagemann, D
Rosenthal, A
Citation: A. Rump et al., Complex arrangement of genes within a 220-kb region of double-duplicated DNA on human 2q37.1, GENOMICS, 73(1), 2001, pp. 50-55
Authors:
Nietzel, A
Rocchi, M
Starke, H
Heller, A
Fiedler, W
Wlodarska, I
Loncarevic, IF
Beensen, V
Claussen, U
Liehr, T
Citation: A. Nietzel et al., A new multicolor-FISH approach for the characterization of marker chromosomes: centromere-specific multicolor-FISH (cenM-FISH), HUM GENET, 108(3), 2001, pp. 199-204
Authors:
Mrasek, K
Heller, A
Rubtsov, N
Trifonov, V
Starke, H
Rocchi, M
Claussen, U
Liehr, T
Citation: K. Mrasek et al., Reconstruction of the female Gorilla gorilla karyotype using 25-color FISHand multicolor banding (MCB), CYTOG C GEN, 93(3-4), 2001, pp. 242-248
Authors:
Liehr, T
Beensen, V
Hauschild, R
Ziegler, M
Hartmann, I
Starke, H
Heller, A
Kahler, C
Schmidt, M
Reiber, W
Hesse, M
Claussen, U
Citation: T. Liehr et al., Pitfalls of rapid prenatal diagnosis using the interphase nucleus, PRENAT DIAG, 21(5), 2001, pp. 419-421
Authors:
Stankiewicz, P
Thiele, H
Giannakudis, I
Schlicker, M
Baldermann, C
Kruger, A
Dorr, S
Starke, H
Hansmann, I
Citation: P. Stankiewicz et al., Kabuki syndrome-like features associated with a small ring chromosome X and XIST gene expression, AM J MED G, 102(3), 2001, pp. 286-292
Authors:
Liehr, T
Beensen, V
Starke, H
Hauschild, R
Hempell, E
Fritsche, V
Hoppe, C
Grosswendt, G
Prechtel, M
Ziegler, M
Claussen, U
von Eggeling, F
Citation: T. Liehr et al., Tetrasomy 21 due to a de novo Robertsonian translocation t(14;21) and an additional free trisomy 21, CLIN GENET, 60(1), 2001, pp. 83-85
Authors:
Starke, H
Raida, M
Trifonov, V
Clement, JH
Loncarevic, IF
Heller, A
Bleck, C
Nietzel, A
Rubtsov, N
Claussen, U
Liehr, T
Citation: H. Starke et al., Molecular cytogenetic characterization of an acquired minute supernumerarymarker chromosome as the sole abnormality in a case clinically diagnosed as atypical Philadelphia-negative chronic myelogenous leukaemia, BR J HAEM, 113(2), 2001, pp. 435-438
Authors:
Eder, E
Puchta, H
Starke, H
Steinhauser, F
Citation: E. Eder et al., The third generation of the remote monitoring system for nuclear reactors in Bavaria, KERNTECHNIK, 65(4), 2000, pp. 152-156
Authors:
Heller, A
Seidel, J
Hubler, A
Starke, H
Beensen, V
Senger, G
Rocchi, M
Wirth, J
Chudoba, I
Claussen, U
Liehr, T
Citation: A. Heller et al., Molecular cytogenetic characterisation of partial trisomy 9q in a case with pyloric stenosis and a review, J MED GENET, 37(7), 2000, pp. 529-532
Authors:
Stankiewicz, P
Bocian, E
Jakubow-Durska, K
Obersztyn, E
Lato, E
Starke, H
Mroczek, K
Mazurczak, T
Citation: P. Stankiewicz et al., Identification of supernumerary marker chromosomes derived from chromosomes 5, 6, 19, and 20 using FISH, J MED GENET, 37(2), 2000, pp. 114-120
Authors:
Liehr, T
Starke, H
Beensen, V
Kahler, C
Harbich, M
Brude, E
Ziegler, M
Claussen, U
Citation: T. Liehr et al., Translocation trisomy dup(21q) and free trisomy 21 can be distinguished byinterphase-FISH, INT J MOL M, 3(1), 1999, pp. 11-14
Authors:
Starke, H
Schreyer, I
Kahler, C
Fiedler, W
Beensen, V
Heller, A
Nietzel, A
Claussen, U
Liehr, T
Citation: H. Starke et al., Molecular cytogenetic characterization of a prenatally detected supernumerary minute marker chromosome 8, PRENAT DIAG, 19(12), 1999, pp. 1169-1174
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