Publikationen von Thomas Haaf

Bartsch, O.; Gebauer, K.; Lechno, S.; van Esch, H.; Froyen, G.; Bonin, M.; Jörg Seidel, J. S.; Thamm-Mücke, B.; Horn, D.; Klopock, E. et al.; Hertzberg, C.; Zechner, U.; Haaf, T.: Four unrelated patients with Lubs X-linked mental retardation syndrome and different Xq28 duplications. American Journal of Medical Genetics Part A 152A (2), S. 305 - 312, (2010)

Haensel, J.; Kohlschmidt, N.; Pitz, S.; Keilmann, A.; Zenker, M.; Ullmann, R.; Haaf, T.; Bartsch, O.: Case report supporting that the Barber-Say and ablepharon macrostomia syndromes could represent one disorder. American Journal of Medical Genetics Part A 149 (10), S. 2236 - 2240 (2009)

Bartsch, O.; Vlccaronková, Z.; Erdogan, F.; Ullmann, R.; Novotná, D.; Spiegel, M.; Beyer, V.; Haaf, T.; Zechner, U.; Seemanová, E.: Two independent chromosomal rearrangements, a very small (550 kb) duplication of the 7q subtelomeric region and an atypical 17q11.2 (NF1) microdeletion, in a girl with neurofibromatosis. Cytogenetic and Genome Research 119 (1 - 2), S. 158 - 64 (2007)

Bartsch, O.; Rasi, S.; Delicado, A.; Dyack, S.; Neumann, L. M.; Seemanová, E.; Volleth, M.; Haaf, T.; Kalscheuer, V. M.: Evidence for a new contiguous gene syndrome, the chromosome 16p13.3 deletion syndrome alias severe Rubinstein–Taybi syndrome. Human Genetics 120 (3), S. 179 - 186 (2006)

Tsend-Ayush, E.; Grützner, F.; Yue, Y.; Grossmann, B.; Hänsel, U.; Sudbrak, R.; Haaf, T.: Plasticity of human chromosome 3 during primate evolution. Genomics 83 (2), S. 193 - 202 (2004)

Lemmers, R. J. L. F.; Osborn, M.; Haaf, T.; Rogers, M.; Frants, R. R.; Padberg, G. W.; Cooper, D. N.; van der Maarel, S. M.; Upadhyaya, M.: D4F104S1 deletion in facioscapulohumeral muscular dystrophy - Phenotype, size, and detection. Neurology 61 (2), S. 178 - 183 (2003)

Grützner, F.; Roest Crollius, H.; Lütjens, G.; Jaillon, O.; Weissenbach, J.; Ropers, H. H.; Haaf, T.: Four-Hundred Million Years of Conserved Synteny of Human Xp and Xq Genes on Three Tetraodon Chromosomes. Genome Research 12 (9), S. 1316 - 1322 (2002)

Voigt, R.; Maier-Weidmann, M.; Lange, P. E.; Haaf, T.: Chromosome 10p13-14 and 22q11 deletion screening in 100 patients with isolated and syndromic conotruncal heart defects. Journal of Medical Genetics 39 (4), S. e16 - e16 (2002)

Raderschall, E.; Bazarov, A.; Cao, J.; Lurz, R.; Smith, A.; Mann, W.; Ropers, H. H.; Sedivy, J. M.; Golub, E. I.; Fritz, E. et al.; Haaf, T.: Formation of higher-order nuclear Rad51 structures is functionally linked to p21 expression and protection from DNA damage-induced apoptosis. Journal of Cell Science 115 (1), S. 153 - 164 (2002)

Raderschall, E.; Bazarov, A.; Cao, J.; Lurz, R.; Smith, A.; Mann, W.; Ropers, H. H.; Sedivy, J. M.; Golub, E. I.; Fritz, E. et al.; Haaf, T.: Formation of higher-order nuclear Rad51 structures is functionally linked to p21 expression and protection from DNA damage-induced apoptosis. Journal of Cell Science 115 (1), S. 153 - 164 (2002)

Raderschall, E.; Stout, K.; Freier, S.; Suckow, V.; Schweiger, S.; Haaf, T.: Elevated Levels of Rad51 Recombination Protein in Tumor Cells. Cancer Research 62 (1), S. 219 - 225 (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)