Publikationen von D. Horn

M. Arelin, B. Schulze, B. Muller-Myhsok, D. Horn, A. Diers, B. Uhlenberg, P. Nurnberg, G. Nurnberg, C. Becker, S. Mundlos, T. H. Lindner, K. Sperling, and K. Hoffmann, "Genome-wide linkage analysis is a powerful prenatal diagnostic tool in families with unknown genetic defects," European journal og human genetics: EJHG ; the official journal of the European Society of Human Genetics 21 (4), 367-372 (2013).

P. Villavicencio-Lorini, E. Klopocki, M. Trimborn, R. Koll, S. Mundlos, and D. Horn, "Phenotypic variant of Brachydactyly-mental retardation syndrome in a family with an inherited interstitial 2q37.3 microdeletion including HDAC4," European journal og human genetics: EJHG ; the official journal of the European Society of Human Genetics 2012, e-e (2012).

P. M. Krawitz, Y. Murakami, J. Hecht, U. Kruger, S. E. Holder, G. R. Mortier, B. Delle Chiaie, E. De Baere, M. D. Thompson, T. Roscioli, S. M. Kielbasa, T. Kinoshita, S. Mundlos, P. N. Robinson, and D. Horn, "Mutations in PIGO, a member of the GPI-anchor-synthesis pathway, cause hyperphosphatasia with mental retardation," American Journal of Human Genetics 91 (1), 146-151 (2012).

E. Klopocki, S. Lohan, S. C. Doelken, S. Stricker, C. W. Ockeloen, R. Soares Thiele de Aguiar, K. Lezirovitz, Mingroni Netto, A. Jamsheer, H. Shah, I. Kurth, R. Habenicht, M. Warman, K. Devriendt, U. Kordass, M. Hempel, A. Rajab, O. Makitie, M. Naveed, U. Radhakrishna, S. E. Antonarakis, D. Horn, and S. Mundlos, "Duplications of BHLHA9 are associated with ectrodactyly and tibia hemimelia inherited in non-Mendelian fashion," Journal of Medical Genetics (London) 49 (2), 119-125 (2012).