Retraction
Identification of a novel RUNX2 gene mutation and early diagnosis of CCD in a cleidocranial dysplasia suspected Iranian family
Paper Information
Record ID:
44864
Journal:
Publication Date:
April 03, 2020
Retraction Date:
August 28, 2020
(5.2 years years ago)
Subjects:
Institutions:
- Medical Genetics Group Department of Experimental Medicine Sapienza'' University of Rome Rome Italy
- Medical Genetics Department DeNA Laboratory Tehran Iran
- U.O.C. of Medical Genetics Policlinic of Tor Vergata Rome Italy
- Universal Scientific Education and Research Network Tehran Iran
- Department of Medical Genetics Faculty of Medical Sciences Tarbiat Modares University Tehran Iran
Article Type:
Publisher:
Wiley
Open Access:
Yes
DOI:
PubMed ID:
Retraction PubMed ID:
Not indexed in PubMed
Retraction Details
Citations (6)
6
Total Citations4
Post-Retraction(66.7%)
1
Pre-Retraction0
Same DayPost-Retraction Citation Analysis
0
Within 30 days
0
Within 1 year
3
After 2+ years
1526
Days since retraction (latest)
Heavy Metals Removal Using Carbon Based Nanocomposites
Unknown Authors
Unknown Journal
Published: Unknown
A novel RUNX2 splice site mutation in Chinese associated with cleidocranial dysplasia
Jing Wang, Qiuying Li, Hongyu Li et al. (7 authors)
Heliyon
Open Access
Published: Nov 2024
1526 days after retraction
A Novel Runx2 Splice Site Mutation in Chinese Associated with Cleidocranial Dysplasia
Jing Wang, Qiuying Li, Hongyu Li et al. (7 authors)
Unknown Journal
Published: Jan 2024
1221 days after retraction
COVID-19 related biliary injury: A review of recent literature
Sujani Yadlapati, Simone A. Jarrett, Daniel Baik et al. (4 authors)
World Journal of Gastroenterology
Open Access
Published: Apr 2023
3 citations
3 citations
957 days after retraction
Manejo odontológico integral de una paciente con disostosis cleidocraneal. Reporte caso
Zoila Beatriz Carbonell–Muñoz, Dacia Malambo‐García, Rossana López Sáleme et al. (5 authors)
Acta Odontológica Colombiana
Open Access
Published: Jul 2022
1 citation
1 citation
686 days after retraction
Identification of a novel RUNX2 gene mutation and early diagnosis of CCD in a cleidocranial dysplasia suspected Iranian family
Omid Daneshjoo, Pirooz Ebrahimi, Leila Salehi et al. (5 authors)
Clinical Case Reports
Open Access
Published: Apr 2020
5 citations
5 citations
147 days before retraction
Quick Stats
Total Citations:
7
Years Since Retraction:
5.2 years
Open Access:
Yes
Last Checked:
Jul 24, 2025