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Results: 1-10 |
Results: 10
Short stature homeobox-containing gene deletion screening by fluorescence in situ hybridisation in patients with short stature
Authors: Musebeck, J Mohnike, K Beye, P Tonnies, H Neitzel, H Schnabel, D Gruters, A Wieacker, PF Stumm, M
Citation: J. Musebeck et al., Short stature homeobox-containing gene deletion screening by fluorescence in situ hybridisation in patients with short stature, EUR J PED, 160(9), 2001, pp. 561-565
Comparative genomic hybridization based strategy for the analysis of different chromosome imbalances detected in conventional cytogenetic diagnostics
Authors: Tonnies, H Stumm, M Wegner, RD Chudoba, I Kalscheuer, V Neitzel, H
Citation: H. Tonnies et al., Comparative genomic hybridization based strategy for the analysis of different chromosome imbalances detected in conventional cytogenetic diagnostics, CYTOG C GEN, 93(3-4), 2001, pp. 188-194
Chromosomal integration pattern of a helper-dependent minimal adenovirus vector with a selectable marker inserted into a 27.4-kilobase genomic stuffer
Authors: Hillgenberg, M Tonnies, H Strauss, M
Citation: M. Hillgenberg et al., Chromosomal integration pattern of a helper-dependent minimal adenovirus vector with a selectable marker inserted into a 27.4-kilobase genomic stuffer, J VIROLOGY, 75(20), 2001, pp. 9896-9908
De novo terminal deletion of chromosome 15q26.1 characterised by comparative genomic hybridisation and FISH with locus specific probes
Authors: Tonnies, H Schulze, I Hennies, HC Neumann, LM Keitzer, R Neitzel, H
Citation: H. Tonnies et al., De novo terminal deletion of chromosome 15q26.1 characterised by comparative genomic hybridisation and FISH with locus specific probes, J MED GENET, 38(9), 2001, pp. 617-621
Molecular cytogenetic characterisation of a complex 46,XY,t(7;8;11;13) chromosome rearrangement in a patient with Moebius syndrome
Authors: Borck, G Wirth, J Hardt, T Tonnies, H Brondum-Nielsen, K Bugge, M Tommerup, N Nothwang, HG Ropers, HH Haaf, T
Citation: G. Borck et al., Molecular cytogenetic characterisation of a complex 46,XY,t(7;8;11;13) chromosome rearrangement in a patient with Moebius syndrome, J MED GENET, 38(2), 2001, pp. 117-120
Analysis of sporadic neuroendocrine rumours of the enteropancreatic systemby comparative genomic hybridisation
Authors: Tonnies, H Toliat, MR Ramel, C Pape, UF Neitzel, H Berger, W Wiedenmann, B
Citation: H. Tonnies et al., Analysis of sporadic neuroendocrine rumours of the enteropancreatic systemby comparative genomic hybridisation, GUT, 48(4), 2001, pp. 536-541
Delineation of a complex karyotypic rearrangement by microdissection and CGH in a family affected with split foot
Authors: Weimer, J Kiechle, M Wiedemann, U Tonnies, H Neitzel, H Ruhenstroth, E Ovens-Raeder, A Arnold, N
Citation: J. Weimer et al., Delineation of a complex karyotypic rearrangement by microdissection and CGH in a family affected with split foot, J MED GENET, 37(6), 2000, pp. 442-445
Molecular cytogenetic techniques for the diagnosis of chromosomal abnormalities in childhood disease
Authors: Stumm, M Tonnies, H Wieacker, PF
Citation: M. Stumm et al., Molecular cytogenetic techniques for the diagnosis of chromosomal abnormalities in childhood disease, EUR J PED, 158(7), 1999, pp. 531-536
Mosaic tetrasomy 9p in a girl with multiple congenital anomalies: cytogenetic and molecular-cytogenetic studies
Authors: Stumm, M Tonnies, H Mandon, U Gotze, A Krebs, P Wieacker, PF
Citation: M. Stumm et al., Mosaic tetrasomy 9p in a girl with multiple congenital anomalies: cytogenetic and molecular-cytogenetic studies, EUR J PED, 158(7), 1999, pp. 571-575
Partial monosomy 2p as the single chromosomal anomaly in a case of renal metanephric adenoma
Authors: Stumm, M Koch, A Wieacker, PF Phillip, C Steinbach, F Allhoff, EP Buhtz, P Walter, H Tonnies, H Wirth, J
Citation: M. Stumm et al., Partial monosomy 2p as the single chromosomal anomaly in a case of renal metanephric adenoma, CANC GENET, 115(1), 1999, pp. 82-85
Risultati: 1-10 |