Cleidocranial dysplasia and novel RUNX2 variants: dental, craniofacial, and osseous manifestations

Abstract Cleidocranial dysplasia (CCD) is a skeletal disorder affecting cranial sutures, teeth, and clavicles, and is associated with the RUNX2 mutations. Although numerous patients have been described, a direct genotype-phenotype correlation for RUNX2 has been difficult to establish. Further cases...

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Main Authors: Sermporn THAWEESAPPHITHAK (Author), Jirawat SAENGSIN (Author), Wuttichart KAMOLVISIT (Author), Thanakorn THEERAPANON (Author), Thantrira PORNTAVEETUS (Author), Vorasuk SHOTELERSUK (Author)
Format: Book
Published: University of São Paulo, 2022-06-01T00:00:00Z.
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3rd Floor Main Library

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Call Number: A1234.567
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