Anthoni, H., L. E. Sucheston, B. A. Lewis, I. Tapia-Paez, X. T. Fan, M. Zucchelli, M. Taipale, C. M. Stein, M. E. Hokkanen, E. Castren, B. F. Pennington, S. D. Smith, R. K. Olson, J. B. Tomblin, G. Schulte-Körne, M. Nöthen, J. Schumacher, B. Müller-Myhsok, P. Hoffmann, J. W. Gilger, G. W. Hynd, J. Nopola-Hemmi, P. H. T. Leppanen, H. Lyytinen, J. Schoumans, M. Nordenskjöld, J. Spencer, D. Stanic, W. C. Boon, E. Simpson, S. Mäkelä, J. A. Gustafsson, M. Peyrard-Janvid, S. Iyengar and J. Kere: The Aromatase Gene CYP19A1: Several Genetic and Functional Lines of Evidence Supporting a Role in Reading, Speech and Language. In: Behavior Genetics 42, 4, 509-527 (2012).
Dahdouh, F., H. Anthoni, I. Tapia-Paez, M. Peyrard-Janvid, G. Schulte-Körne, A. Warnke, H. Remschmidt, A. Ziegler, J. Kere, B. Müller-Myhsok, M. M. Nöthen, J. Schumacher and M. Zucchelli: Further evidence for DYX1C1 as a susceptibility factor for dyslexia. In: Psychiatric Genetics 19, 2, 59-63 (2009).
Ludwig, K. U., J. Schumacher, G. Schulte-Körne, I. R. König, A. Warnke, E. Plume, H. Anthoni, M. Peyrard-Janvid, H. Meng, A. Ziegler, H. Remschmidt, J. Kere, J. R. Gruen, B. Mueller-Myhsok, M. M. Nöthen and P. Hoffmann: Investigation of the DCDC2 intron 2 deletion/compound short tandem repeat polymorphism in a large German dyslexia sample. In: Psychiatric Genetics 18, 6, 310-312 (2008).
Anthoni, H., M. Zucchelli, H. Matsson, B. Müller-Myhsok, I. Fransson, J. Schumacher, S. Massinen, P. Onkamo, A. Warnke, H. Griesemann, P. Hoffmann, J. Nopola-Hemmi, H. Lyytinen, G. Schulte-Koerne, J. Kere, M. M. Nothen and M. Peyrard-Janvid: A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia. In: Human Molecular Genetics 16, 6, 667-677 (2007).
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