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
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