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RUNX2
NM_001024630.4:p.A77_R92delFs
Associated Papers
The impact of RUNX2 gene variants on cleidocranial dysplasia phenotype: a systematic review.
Thaweesapphithak S et al.
Journal of Translational Medicine, 2024
39627759 (PubMed )
Supplement: 12967_2024_5904_MOESM1_ESM.xlsx › Supplement_table_1.
A Novel 90-kbp Deletion of RUNX2 Associated with Cleidocranial Dysplasia.
Zhang Y et al.
Genes, 2022
Deletions of the RUNX2 gene are present in about 10% of individuals with cleidocranial dysplasia.
Ott CE et al.
Human Mutation, 2010
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