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Deletions of the RUNX2 gene are present in about 10% of individuals with cleidocranial dysplasia
Authors: Ott, C. E.; Leschik, G.; Trotier, F.; Brueton, L.; Brunner, H. G.; Brussel, W.; Guillen-Navarro, E.; Haase, C.; Kohlhase, J.; Kotzot, D.; Lane, A.; Lee-Kirsch, M. A.; Morlot, S.; Simon, M. E.; Steichen-Gersdorf, E.; Tegay, D. H.; Peters, H.; Mundlos, S.; Klopocki, E.
Date of Publication (YYYY-MM-DD): 2010-06-03
Title of Journal: Human Mutation
Volume: 31
Issue / Number: 8
Start Page: E1587
End Page: 93
Document Type: Article
ID: 539733.0
 
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