Abstract

The above article from Clinical Case Reports, published online on 3 April 2020 in Wiley Online Library as Early View (https://onlinelibrary.wiley.com/doi/full/10.1002/ccr3.2825), has been retracted by agreement between Dr Masoud Garshasbi, the Editor‐in‐Chief and John Wiley and Sons Ltd. The retraction has been agreed because the article has been submitted and approved for publication by Dr. Omid Daneshjoo without consent in any form from the named co‐authors and Dr. Masoud Garshasbi. Reference Daneshjoo O, Ebrahimi P, Salehi LB, Pizzuti A, Garshasbi M. Identification of a novel RUNX2 gene mutation and early diagnosis of CCD in a cleidocranial dysplasia suspected Iranian family (2020). Clin Case Rep. 2020;1‐8.

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