Buonincontri, R., I. Bache, A. Silahtaroglu, C. Elbro, A.-M. Veber Nielsen, R. Ullmann, G. Arkesteijn and N. Tommerup: Cohort of Balanced Reciprocal Translocations Associated with Dyslexia: Identification of Two Putative Candidate Genes at DYX1.. In: Behavior Genetics: an International Journal Devoted to Research in the Inheritance of Behavior in Animals and man 41, 1, 125-133 (2010).
url: http://www.springerlink.com/content/8617511w5k714446/fulltext.pdf
doi: 10.1007/s10519-010-9389-2
Hilhorst-Hofstee, Y., Z. Tümer, P. Born, J. Knijnenburg, K. Hansson, V. Yatawara, J. Steensberg, R. Ullmann, G. Arkesteijn, N. Tommerup and L. A. Larsen: Molecular characterization of two patients with de novo interstitial deletions in 4q22-q24. In: American Journal of Medical Genetics Part A 149, 8, 1830-1833 (2009).
doi: 10.1002/ajmg.a.32977
url: http://www3.interscience.wiley.com/cgi-bin/fulltext/122514813/PDFSTART
Chen, W., V. Kalscheuer, A. Tzschach, C. Menzel, R. Ullmann, M. H. Schulz, F. Erdogan, L. Na, Z. Kijas, G. Arkesteijn, I. L. Pajares, M. Goetz-Sothmann, U. Heinrich, I. Rost, A. Dufke, U. Grasshoff, B. Glaeser, M. Vingron and H. H. Ropers: Mapping translocation breakpoints by next-generation sequencing. In: Genome Research 18, 7, 1143-1149 (2008).
url: http://genome.cshlp.org/content/18/7/1143.abstract
doi: 10.1101/gr.076166.108
Kalscheuer, V. M., D. FitzPatrick, N. Tommerup, M. Bugge, E. Niebuhr, L. M. Neumann, A. Tzschach, S. A. Shoichet, C. Menzel, F. Erdogan, G. Arkesteijn, H.-H. Ropers and R. Ullmann: Mutations in Autism Susceptibility Candidate 2 (AUTS2) in patients with mental retardation. In: Human Genetics 121, 3-4, 501-509 (2007).
doi: 10.1007/s00439-006-0284-0
url: http://www.springerlink.com/content/f503q876832m2404/fulltext.pdf
The Max Planck Society does not take any responsibility for the content of this export.