Horn, D., J. Kapeller, N. Rivera-Brugues, U. Moog, B. Lorenz-Depiereux, S. Eck, M. Hempel, J. Wagenstaller, A. Gawthrope, A. P. Monaco, M. Bonin, O. Riess, E. Wohlleber, T. Illig, C. R. Bezzina, A. Franke, S. Spranger, P. Villavicencio-Lorini, W. Seifert, J. Rosenfeld, E. Klopocki, G. A. Rappold and T. M. Strom: Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits. In: Human Mutation 31, 11, E1851-E1860 (2010).
url: http://www.ncbi.nlm.nih.gov/pubmed/20848658
doi: 10.1002/humu.21362
Zimprich, F., E. Stogmann, S. Bonelli, C. Baumgartner, J. C. Mueller, T. Meitinger, A. Zimprich and T. M. Strom: A functional polymorphism in the SCN1A gene is not associated with carbamazepine dosages in Austrian patients with epilepsy. In: Epilepsia 49, 6, 1108-1109 (2008).
Mijalski, T., A. Harder, T. Halder, M. Kersten, M. Horsch, T. M. Strom, H. V. Liebscher, F. Lottspeich, M. H. de Angelis and J. Beckers: Identification of coexpressed gene clusters in a comparative analysis of transcriptome and proteome in mouse tissues. In: Proceedings of the National Academy of Sciences of the United States of America 102, 24, 8621-8626 (2005).
Zimprich, A., S. Biskup, P. Leitner, P. Lichtner, M. Farrer, S. Lincoln, J. Kachergus, M. Hulihan, R. J. Uitti, D. B. Calne, A. J. Stoessl, R. F. Pfeiffer, N. Patenge, I. C. Carbajal, P. Vieregge, F. Asmus, B. Müller-Myhsok, D. W. Dickson, T. Meitinger, T. M. Strom, Z. K. Wszolek and T. Gasser: Mutations in LRRK2 cause autosomal-dominant Parkinsonism with pleomorphic pathology. In: Neuron 44, 4, 601-607 (2004).
Winkelmann, J., P. Lichtner, T. M. Strom, C. Trenkwalder, T. Meitinger and B. Müller-Myhsok: Evidence for genetic heterogeneity in Restless Legs Syndrome. In: Pharmacopsychiatry 36, 5, 273-273 (2003).
Binder, E. B., P. Lichtner, M. Uhr, T. Bettecken, T. M. Strom, T. Meitinger, S. Modell and F. Holsboer: Mutation analysis of genes regulating the hypothalamo-pituitary adrenal (HPA) axis in patients with depressive syndrome.. In: American Journal of Human Genetics 71, 4 Suppl. Suppl. S, 468-468 (2002).
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