Deletions of the RUNX2 gene are present in about 10% of individuals with cleidocranial dysplasia
- DOI
- 10.1002/humu.21298
- Published
- 2010-06-03
- Container
- Human Mutation
- Publisher
- Hindawi Limited
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1002/humu.21298,
title = {Deletions of the RUNX2 gene are present in about 10\% of individuals with cleidocranial dysplasia},
author = {Claus E. Ott and Gundula Leschik and Fabienne Trotier and Louise Brueton and Han G. Brunner and Wim Brussel and Encarna Guillen-Navarro and Claudia Haase and Juergen Kohlhase and Dieter Kotzot and Andrew Lane and Min Ae Lee-Kirsch and Susanne Morlot and Marleen E.H. Simon and Elisabeth Steichen-Gersdorf and David H. Tegay and Hartmut Peters and Stefan Mundlos and Eva Klopocki},
year = {2010},
journal = {Human Mutation},
doi = {10.1002/humu.21298},
url = {https://doi.org/10.1002/humu.21298}
}RIS
TY - JOUR TI - Deletions of the RUNX2 gene are present in about 10% of individuals with cleidocranial dysplasia AU - Claus E. Ott AU - Gundula Leschik AU - Fabienne Trotier AU - Louise Brueton AU - Han G. Brunner AU - Wim Brussel AU - Encarna Guillen-Navarro AU - Claudia Haase AU - Juergen Kohlhase AU - Dieter Kotzot AU - Andrew Lane AU - Min Ae Lee-Kirsch AU - Susanne Morlot AU - Marleen E.H. Simon AU - Elisabeth Steichen-Gersdorf AU - David H. Tegay AU - Hartmut Peters AU - Stefan Mundlos AU - Eva Klopocki PY - 2010 JO - Human Mutation DO - 10.1002/humu.21298 UR - https://doi.org/10.1002/humu.21298 ER -
APA
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. (2010). Deletions of the RUNX2 gene are present in about 10% of individuals with cleidocranial dysplasia. Human Mutation. https://doi.org/10.1002/humu.21298
Source records
- crossref · retrieved 2026-09-25T11:43:26.251Z