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
Gilling, M., M. B. Lauritsen, M. Møller, K. F. Henriksen, A. Vicente, G. Oliveira, C. Cintin, H. Eiberg, P. S. Andersen, O. Mors, T. Rosenberg, K. Brøndum-Nielsen, R. M. J. Cotterill, C. Lundsteen, H.-H. Ropers, R. Ullmann, I. Bache, Z. Tümer and N. Tommerup: A 3.2 Mb deletion on 18q12 in a patient with childhood autism and high-grade myopia.. In: European Journal of Human Genetics 16, 3, 312-319 (2008).
url: translocation, deletion, autism, myopia, array CGH, chromosome 18
doi: 10.1038/sj.ejhg.5201985
Belloso, J. M., I. Bache, M. Guitart, M. R. Caballin, C. Halgren, M. Kirchhoff, H.-H. Ropers, N. Tommerup and Z. Tümer: Disruption of the CNTNAP2 gene in a t(7;15) translocation family without symptoms of Gilles de la Tourette syndrome. In: European Journal og Human Genetics : EJHG ; the Official Journal of the European Society of Human Genetics 15, 6, 711-713 (2007).
doi: :10.1038/sj.ejhg.5201824
Bache, I., E. Van Assche, S. Cingoz, M. Bugge, Z. Tümer, M. Hjorth, C. Lundsteen, J. Lespinasse, K. Winther, A. Niebuhr, V. Kalscheuer, I. Liebaers, M. Bonduelle, H. Tournaye, C. Ayuso, G. Barbi, E. Blennow, G. Bourrouillou, K. Brondum-Nielsen, G. Bruun-Petersen, M.-F. Croquette, S. Dahoun, B. Dallapiccola, V. Davison, B. Delobel, H.-C. Duba, L. Duprez, M. Ferguson-Smith, D. R. FitzPatrick, E. Grace, I. Hansmann, M. Hultén, P. K. A. Jensen, P. Jonveaux, U. Kristoffersson, I. Lopez-Pajares, J. McGowan-Jordan, J. Murken, M. Orera, T. Parkin, E. Passarge, C. Ramos, K. Rasmussen, W. Schempp, R. Schubert, E. Schwinger, F. Shabtai, K. Smith, R. Stallings, M. Stefanova, L. Tranebjerg, C. Turleau, C. B. van der Hagen, M. Vekemans, N. K. Vokac, K. Wagner, J. Wahlstroem, L. Zelante and N. Tommerup: An excess of chromosome 1 breakpoints in male infertility. In: European Journal of Human Genetics 12, 12, 993-1000 (2004).
doi: 10.1038/sj.ejhg.5201263
http://edoc.mpg.de
The Max Planck Society does not take any responsibility for the content of this export.