Identification of a novel RUNX2 gene mutation and early diagnosis of CCD in a cleidocranial dysplasia suspected Iranian family.

Daneshjoo O, Ebrahimi P, Salehi LB, Pizzuti A, Garshasbi M

DOI: 10.1002/ccr3.2825
Published: 2020 Dec
Container: Clinical case reports
Publisher: Not recorded
Open access: yes

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Cite this work

BibTeX

@article{allodium:10.1002/ccr3.2825,
  title = {Identification of a novel RUNX2 gene mutation and early diagnosis of CCD in a cleidocranial dysplasia suspected Iranian family.},
  author = {Daneshjoo O and Ebrahimi P and Salehi LB and Pizzuti A and Garshasbi M},
  year = {2020},
  journal = {Clinical case reports},
  doi = {10.1002/ccr3.2825},
  url = {https://doi.org/10.1002/ccr3.2825}
}

RIS

TY  - JOUR
TI  - Identification of a novel RUNX2 gene mutation and early diagnosis of CCD in a cleidocranial dysplasia suspected Iranian family.
AU  - Daneshjoo O
AU  - Ebrahimi P
AU  - Salehi LB
AU  - Pizzuti A
AU  - Garshasbi M
PY  - 2020
JO  - Clinical case reports
DO  - 10.1002/ccr3.2825
UR  - https://doi.org/10.1002/ccr3.2825
ER  -

APA

O, D., P, E., LB, S., A, P., & M, G. (2020). Identification of a novel RUNX2 gene mutation and early diagnosis of CCD in a cleidocranial dysplasia suspected Iranian family.. Clinical case reports. https://doi.org/10.1002/ccr3.2825

Source records

pubmed · retrieved 2026-09-25T00:54:54.342Z
europe-pmc · retrieved 2026-09-25T00:54:54.365Z
doaj · retrieved 2026-09-25T00:54:54.347Z