Übersicht der Publikationen

Zeitschriftenartikel (7)

Brunner, B.; Hornung, U.; Shan, Z.; Nanda, I.; Kondo, M.; Zend-Ajusch, E.; Haaf, T.; Ropers, H. H.; Shima, A.; Schmid, M. et al.; Kalscheuer, V. M.; Schartl, M.: Genomic organization and expression of the doublesex-related gene cluster in vertebrates and detection of putative regulatory regions for DMRT1. Genomics 77 (1-2), S. 8 - 17 (2001)
Fritz, B.; Aslan, M.; Kalscheuer, V.; Ramsing, M.; Saar, K.; Fuchs, B.; Rehder, H.: Low incidence of UPD in spontaneous abortions beyond the 5th gestational week. Eur J Hum Genet 9 (12), S. 910 - 6 (2001)
Mergenthaler, S.; Hitchins, M. P.; Blagitko-Dorfs, N.; Monk, D.; Wollmann, H. A.; Ranke, M. B.; Ropers, H. H.; Apostolidou, S.; Stanier, P.; Preece, M. A. et al.; Eggermann, T.; Kalscheuer, V. M.; Moore, G. E.: Conflicting reports of imprinting status of human GRB10 in developing brain: how reliable are somatic cell hybrids for predicting allelic origin of expression? Am J Hum Genet 68 (2), S. 543 - 5 (2001)
Mergenthaler, S.; Sharp, A.; Ranke, M. B.; Kalscheuer, V. M.; Wollmann, H. A.; Eggermann, T.: Gene dosage analysis in Silver-Russell syndrome: use of quantitative competitive PCR and dual-color FISH to estimate the frequency of duplications in 7p11.2-p13. Genet Test 5 (3), S. 261 - 6 (2001)
Sudbrak, R.; Wieczorek, G.; Nuber, U. A.; Mann, W.; Kirchner, R.; Erdogan, F.; Brown, C. J.; Wohrle, D.; Sterk, P.; Kalscheuer, V. M. et al.; Berger, W.; Lehrach, H.; Ropers, H. H.: X chromosome-specific cDNA arrays: identification of genes that escape from X-inactivation and other applications. Hum Mol Genet 10 (1), S. 77 - 83 (2001)
Tonnies, H.; Stumm, M.; Wegner, R. D.; Chudoba, I.; Kalscheuer, V.; Neitzel, H.: Comparative genomic hybridization based strategy for the analysis of different chromosome imbalances detected in conventional cytogenetic diagnostics. Cytogenet Cell Genet 93 (3-4), S. 188 - 94 (2001)
Volleth, M.; Stumm, M.; Mohnike, K.; Kalscheuer, V. M.; Jakubiczka, S.; Wieacker, P.: Preferential inactivation of a dupX(q23 --> q27-28) chromosome in a girl with mental retardation and dysmorphy. Hum Hered 52 (3), S. 177 - 82 (2001)
Zur Redakteursansicht