Associated Papers
Cleidocranial dysplasia with severe parietal bone dysplasia: C-terminal RUNX2 mutations.
Cunningham ML et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology, 2006
Six novel mutations of the RUNX2 gene in Italian patients with cleidocranial dysplasia.
Tessa A et al.
Human Mutation, 2003
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