Identification of a novel RUNX2 gene mutation and early diagnosis of CCD in a cleidocranial dysplasia suspected Iranian family
- Type
- Retraction
- Notice date
- 8/28/2020 0:00
- Journal
- Clinical Case Reports
- Publisher
- Wiley
- Notice DOI
- 10.1002/ccr3.3178
- Original paper DOI
- 10.1002/ccr3.2825