Publikationen von F. Trotier

C. E. Ott, G. Leschik, F. Trotier, L. Brueton, H. G. Brunner, W. Brussel, E. Guillen-Navarro, C. Haase, J. Kohlhase, D. Kotzot, A. Lane, M. A. Lee-Kirsch, S. Morlot, M. E. Simon, E. Steichen-Gersdorf, D. H. Tegay, H. Peters, S. Mundlos, and E. Klopocki, "Deletions of the RUNX2 gene are present in about 10% of individuals with cleidocranial dysplasia," Human Mutation 31 (8), E1587-93 (2010).

Eva Klopocki, Harald Schulze, Gabriele Strauß, Claus-Eric Ott, Judith Hall, Fabienne Trotier, Silke Fleischhauer, Lynn Greenhalgh, Ruth A. Newbury-Ecob, Luitgard M. Neumann, Rolf Habenicht, Rainer König, Eva Seemanova, André Megarbane, Hans-Hilger Ropers, Reinhard Ullmann, and Stefan Mundlos, "Complex inheritance pattern resembling autosomal recessive inheritance involving a microdeletion in thrombocytopenia-absent radius," American Journal of Human Genetics: AJHG / American Society of Human Genetics 80 (2), 232-240 (2007).

Eva Klopocki, Harald Schulze, Gabriele Strauß, Claus-Eric Ott, Judith Hall, Fabienne Trotier, Silke Fleischhauer, Lynn Greenhalgh, Ruth A. Newbury-Ecob, Luitgard M. Neumann, Rolf Habenicht, Rainer König, Eva Seemanova, André Megarbane, Hans-Hilger Ropers, Reinhard Ullmann, and Stefan Mundlos, "Complex inheritance pattern resembling autosomal recessive inheritance involving a microdeletion in thrombocytopenia-absent radius," American Journal of Human Genetics: AJHG / American Society of Human Genetics 80 (2), 232-240 (2007).