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Highlighting the therapeutic implications of these findings, in utero antioxidant therapy stabilized RUNX2 and improved bone development in the Runx2+/ haplo-insufficient mouse model of human cleidocranial dysplasia

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[DOI] [PMC free article] [PubMed] [Google Scholar] 158.Hollander P., Gupta A.K., Plodkowski R., et al

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