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RUNX2 gene status in a cleidocranial dysplasia patient without supernumerary teeth.

Anthonappa, Robert P

RUNX2 gene status in a cleidocranial dysplasia patient without supernumerary teeth. [electronic resource] - Journal of investigative and clinical dentistry May 2013 - 124-7 p. digital

Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't

ISSN: 2041-1626

Standard No.: 10.1111/jicd.12019 doi

Subjects--Topical Terms:
Child
Cleidocranial Dysplasia--genetics
Core Binding Factor Alpha 1 Subunit--genetics
Female
Humans
Pedigree
Tooth, Supernumerary--genetics

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