Publikationen von D. Seelow

S. Baasanjav, L. Al-Gazali, T. Hashiguchi, S. Mizumoto, B. Fischer, D. Horn, D. Seelow, B. R. Ali, S. A. Aziz, R. Langer, A. A. Saleh, C. Becker, G. Nurnberg, V. Cantagrel, J. G. Gleeson, D. Gomez, J. B. Michel, S. Stricker, T. H. Lindner, P. Nurnberg, K. Sugahara, S. Mundlos, and K. Hoffmann, "Faulty initiation of proteoglycan synthesis causes cardiac and joint defects," Am J Hum Genet 89 (1), 15-27 (2011).

Peter N. Robinson, Sebastian Köhler, Sebastian Bauer, Dominik Seelow, Denise Horn, and Stefan Mundlos, "The Human Phenotype Ontology: A Tool for Annotating and Analyzing Human Hereditary Disease," The American Journal of Human Genetics 83 (5), 610-615 (2008).

Anne Michalk1, Sigmar Stricker, Jutta Becker, Rosemarie Rupps, Tapio Pantzar, Jan Miertus, Giovanni Botta, Valeria G. Naretto, Catrin Janetzki, Nausheen Yaqoob, Claus-Eric Ott, Dominik Seelow, Dagmar Wieczorek, Britta Fiebig, Brunhilde Wirth, Markus Hoopmann, Marisa Walther, Friederike Körber, Markus Blankenburg, Stefan Mundlos, Raoul Heller, and Katrin Hoffmann, "Acetylcholine receptor pathway mutations explain various fetal akinesia deformation sequence disorders," The American Journal of Human Genetics, 82 (2), 464-476 (2008).

Dominik Seelow, Raffaello Galli, Sigrun Mebus, Hans-Peter Sperling, Hans Lehrach, and Silke Sperling, "d-matrix – database exploration, visualization and analysis," BMC Bioinformatics 5, 168-168 (2004).

Bogac Kaynak, Anja von Heydebreck, Sigrun Mebus, Dominik Seelow, Steffen Hennig, Jan Vogel, Hans-Peter Sperling, Reinhard Pregla, Vladimir Alexi-Meskishvili, Roland Hetzer, Peter E. Lange, Martin Vingron, Hans Lehrach, and Silke Sperling, "Genome-wide array analysis of normal and malformed human hearts," Circulation 107 (19), 2467-2474 (2003).