Publikationen von P. Villavicencio-Lorini

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).

C. E. Ott, H. Hein, S. Lohan, J. Hoogeboom, N. Foulds, J. Grunhagen, S. Stricker, P. Villavicencio-Lorini, E. Klopocki, and S. Mundlos, "Microduplications upstream of MSX2 are associated with a phenocopy of cleidocranial dysplasia," Journal of Medical Genetics (London) 49 (7), 437-441 (2012).

D. Horn, 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," Human Mutation 31 (11), E1851-E1860 (2010).

P. Villavicencio-Lorini, P. Kuss, J. Friedrich, J. Haupt, M. Farooq, S. Turkmen, D. Duboule, J. Hecht, and S. Mundlos, "Homeobox genes d11-d13 and a13 control mouse autopod cortical bone and joint formation.," Journal of Clinical Investigation 120 (6), 1994-2004 (2010).

Pia Kuss, Pablo Villavicencio-Lorini, Florian Witte, Joachim Klose, Andrea N. Albrecht, Petra Seemann, Jochen Hecht, and Stefan Mundlos, "Mutant Hoxd13 induces extra digits in a mouse model of synpolydactyly directly and by decreasing retinoic acid synthesis," Journal of Clinical Investigation 119 (1), 146-156 (2009).