Authors:
Petek, E
Kostl, G
Rauter, L
Mutz, I
Wagner, K
Kroisel, PM
Citation: E. Petek et al., Molecular cytogenetics and phenotype characterization of a de novo pure partial trisomy 10(q24.33-qter), CLIN DYSMOR, 10(2), 2001, pp. 151-153
Authors:
Cheung, J
Petek, E
Nakabayashi, K
Tsui, LC
Vincent, JB
Scherer, SW
Citation: J. Cheung et al., Identification of the human cortactin-binding protein-2 gene from the autism candidate region at 7q31, GENOMICS, 78(1-2), 2001, pp. 7-11
Authors:
Emberger, W
Behmel, A
Tschernigg, M
Seewann, HL
Petek, E
Kroisel, PM
Wagner, K
Citation: W. Emberger et al., Chronic myeloid leukemia with a rare variant Philadelphia translocation: t(9;10;22)(q34;q22;q11), CANC GENET, 129(1), 2001, pp. 76-79
Authors:
Emberger, W
Petek, E
Kroisel, PM
Zierler, H
Wagner, K
Citation: W. Emberger et al., Clinical and molecular cytogenetic characterization of two patients with partial trisomy 1q41-qter: Further delineation of partial trisomy 1q syndrome, AM J MED G, 104(4), 2001, pp. 312-318
Authors:
Petek, E
Windpassinger, C
Vincent, JB
Cheung, J
Boright, AP
Scherer, SW
Kroisel, PM
Wagner, K
Citation: E. Petek et al., Disruption of a novel gene (IMMP2L) by a breakpoint in 7q31 associated with Tourette syndrome, AM J HU GEN, 68(4), 2001, pp. 848-858
Authors:
Petek, E
Windpassinger, C
Egger, H
Kroisel, PM
Wagner, K
Citation: E. Petek et al., Localization of the human anterior gradient-2 gene (AGR2) to chromosome band 7p21.3 by radiation hybrid mapping and fluorescence in situ hybridisation, CYTOG C GEN, 89(3-4), 2000, pp. 141-142
Authors:
Emberger, W
Windpassinger, C
Petek, E
Kroisel, PM
Wagner, K
Citation: W. Emberger et al., Assignment of the human GABAA receptor delta-subunit gene (GABRD) to chromosome band 1p36.3 distal to marker NIB1364 by radiation hybrid mapping, CYTOG C GEN, 89(3-4), 2000, pp. 281-282
Authors:
Petek, E
Wagner, K
Steiner, H
Schaffer, H
Kroisel, PM
Citation: E. Petek et al., Prenatal diagnosis of partial trisomy 4q26-qter and monosomy for the Wolf-Hirschhorn critical region in a fetus with split hand malformation, PRENAT DIAG, 20(4), 2000, pp. 349-352
Authors:
Emberger, W
Petek, E
Plecko-Startinig, B
Kroisel, PM
Zierler, H
Wagner, K
Citation: W. Emberger et al., A de novo complex chromosomal rearrangement involving chromosomes 2, 3, and 10 associated with microcephaly and early onset spasticity, J MED GENET, 37(11), 2000, pp. 892-896
Authors:
Auer-Grumbach, M
Loscher, WN
Wagner, K
Petek, E
Korner, E
Offenbacher, H
Hartung, HP
Citation: M. Auer-grumbach et al., Phenotypic and genotypic heterogeneity in hereditary motor neuronopathy type V - A clinical, electrophysiological and genetic study, BRAIN, 123, 2000, pp. 1612-1623