Schickel, J.; Stahn, K.; Zimmer, K.-P.; Sudbrak, R.; Størm, T. M.; Dürst, M.; Kiehntopf, M.; Deufel, T.: Gene for integrin-associated protein (IAP, CD47): physical mapping, genomic structure, and expression studies in skeletal muscle. Biochemistry and Cell Biology 80 (2), S. 169 - 176 (2002)

van Geel, M.; Eichler, E. E.; Beck, A. F.; Shan, Z.; Haaf, T.; van der Maarel, S. M.; Frants, R. R.; de Jong, P. J.: A Cascade of Complex Subtelomeric Duplications during the Evolution of the Hominoid and Old World Monkey Genomes. American Journal of Human Genetics 70 (1), S. 269 - 278 (2002)

Yntema, H. G.; Oudakker, A. R.; Kleefstra, T.; Hamel, B. C. J.; van Bokhoven, H.; Chelly, J.; Kalscheuer, V. M.; Fryns, J.-P.; Raynaud, M.; Moizard, M.-P. et al.; Moraine, C.: In-frame deletion in MECP2 causes mild nonspecific mental retardation. American Journal of Medical Genetics 107 (1), S. 81 - 83 (2002)

Zintzaras, E.; Bouka, P.; Kowald, A.: Biometrical evaluation of bioequivalence trials using a bootstrap individual direct curve comparison method. European Journal of Drug Metabolism and Pharmacokinetics 27 (1), S. 11 - 16 (2002)

Daiber, A.; Nauser, T.; Takaya, N.; Kudo, T.; Weber, P.; Hultschig, C.; Shoun, H.; Ullrich, V.: Isotope effects and intermediates in the reduction of NO by P450NOR. Journal of Inorganic Biochemistry 88 (3 - 4), S. 343 - 352 (2001)

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)

Blagitko, N.; Mergenthaler, S.; Schulz, U.; Wollmann, H. A.; Craigen, W.; Eggermann, T.; Ropers, H. H.; Kalscheuer, V. M.: Human GRB10 is imprinted and expressed from the paternal and maternal allele in a highly tissue- and isoform-specific fashion. Hum Mol Genet 9 (11), S. 1587 - 95 (2000)

Brunner, B.; Grutzner, F.; Yaspo, M. L.; Ropers, H. H.; Haaf, T.; Kalscheuer, V. M.: Molecular cloning and characterization of the Fugu rubripes MEST/COPG2 imprinting cluster and chromosomal localization in Fugu and Tetraodon nigroviridis. Chromosome Res 8 (6), S. 465 - 76 (2000)

Mergenthaler, S.; Blagitko-Dorfs, N.; Wollmann, H. A.; Ranke, M. B.; Ropers, H. H.; Kalscheuer, V. M.; Eggermann, T.: Identification of two new polymorphisms (c2447-125A>G; c2532G>A) in the gamma 2-COP (COPG2) gene by screening of Silver-Russell syndrome patients. Hum Mutat 16 (1), S. 96 (2000)

Singh, A.; Henschel, S.; Sperling, K.; Kalscheuer, V.; Neitzel, H.: Differences in the meiotic pairing behavior of gonosomal heterochromatin between female and male Microtus agrestis: implications for the mechanism of heterochromatin amplification on the X and Y. Cytogenet Cell Genet 91 (1-4), S. 253 - 60 (2000)

Blagitko, N.; Schulz, U.; Schinzel, A. A.; Ropers, H. H.; Kalscheuer, V. M.: gamma2-COP, a novel imprinted gene on chromosome 7q32, defines a new imprinting cluster in the human genome. Hum Mol Genet 8 (13), S. 2387 - 96 (1999)

Brunner, B.; Todt, T.; Lenzner, S.; Stout, K.; Schulz, U.; Ropers, H. H.; Kalscheuer, V. M.: Genomic structure and comparative analysis of nine Fugu genes: conservation of synteny with human chromosome Xp22.2-p22.1. Genome Res 9 (5), S. 437 - 48 (1999)

Krause, R.; Hemberger, M.; Himmelbauer, H.; Kalscheuer, V.; Fundele, R. H.: Identification and characterization of G90, a novel mouse RNA that lacks an extensive open reading frame. Gene 232 (1), S. 35 - 42 (1999)

van de Wetering, R. A.; Gabreels-Festen, A. A.; Kremer, H.; Kalscheuer, V. M.; Gabreels, F. J.; Mariman, E. C.: Regulation and expression of the murine PMP22 gene. Mamm Genome 10 (4), S. 419 - 22 (1999)