Ott, C. E., 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. In: Human Mutation 31, 8, E1587-93 (2010).
url: http://www.ncbi.nlm.nih.gov/pubmed/20648631
doi: 10.1002/humu.21298
Has, C., R. J. Ludwig, C. Herz, J. S. Kern, S. Ussar, F. R. Ochsendorf, R. Kaufmann, H. Schumann, J. Kohlhase and L. Bruckner-Tuderman: C-terminally truncated kindlin-1 leads to abnormal adhesion and migration of keratinocytes. In: British Journal of Dermatology 159, 5, 1192-1196 (2008).
Netzer, C., S. K. Bohlander, L. Rieger, S. Muller and J. Kohlhase: Interaction of the developmental regulator SALL1 with UBE2I and SUMO-1. In: Biochemical and Biophysical Research Communications 296, 4, 870-876 (2002).
Kohlhase, J., A. Koehler, H. Jaeckle, W. Engel and R. Stick: Molecular cloning of a SALL1-related pseudogene and mapping to chromosome Xp11.2.. In: Cytogenetics and Cell Genetics 84, 31-34 (1999).
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