DOI:
10.1055/s-00046370
Global Medical Genetics
LinksClose Window
References
Ott CE, Leschik G, Trotier F. et al.
Deletions of the RUNX2 gene are present in about 10% of individuals with cleidocranial dysplasia.
Hum Mutat 2010;
31 (08) E1587-E1593
Access:
Access:
We do not assume any responsibility for the contents of the web pages of other providers.