Molecular Genetics of Cleidocranial Dysplasia-Reference-Cited by-同舟云学术

Molecular Genetics of Cleidocranial Dysplasia

Published:2020-01-26 Issue:5 Volume:40 Page:442-454
ISSN:1551-3815
Container-title:Fetal and Pediatric Pathology
language:en
Short-container-title:Fetal and Pediatric Pathology

Author:

Motaei Jamshid¹,Salmaninejad Arash¹²^ORCID,Jamali Ebrahim³,Khorsand Imaneh⁴,Ahmadvand Mohammad⁵,Shabani Sasan⁶,Karimi Farshid⁷,Nazari Mohammad Sadegh⁸,Ketabchi Golsa⁹,Naqipour Fatemeh⁹^ORCID

Affiliation:

1. Department of Medical Genetics, Medical Genetics Research Center, Student Research Committee, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran

2. Halal Research Center of IRI, FDA, Tehran, Iran

3. Department of Biology, Tonekabon Branch, Islamic Azad University, Tonekabon, Iran

4. Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran

5. Hematology-Oncology and Stem Cell Transplantation Research Center, Tehran University of Medical Sciences, Tehran, Iran

6. Department of Optometry, School of Para Medical Sciences, Mashhad University of Medical Sciences, Mashhad, Iran

7. Department of Medical Genetics, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran

8. Postgraduate Student, Department of Orthodontics, School of Dentistry, Mashhad University of Medical Science, Mashhad, Iran

9. Postgraduate Student, Department of Oral and Maxillofacial Radiology, School of Dentistry, Mashhad University of Medical Science, Mashhad, Iran

Publisher

Informa UK Limited

Subject

General Medicine,Pathology and Forensic Medicine,Pediatrics, Perinatology, and Child Health

Link

https://www.tandfonline.com/doi/pdf/10.1080/15513815.2019.1710792

Reference62 articles.

1. Delayed Eruption of Permanent Dentition and Maxillary Contraction in Patients with Cleidocranial Dysplasia: Review and Report of a Family

2. Cleidocranial dysplasia: Part 1–General principles of the orthodontic and surgical treatment modality

3. Cleido-cranial Dysostosis — Skeletal Abnormalities

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1. A novel de novo variant in the RUNX2 gene causes cleidocranial dysplasia in a Malian girl;Clinical Case Reports;2024-02

2. Continuous supernumerary teeth development in cleidocranial dysplasia post-surgical extraction – A novel case report;Advances in Oral and Maxillofacial Surgery;2023-12

3. Cleidocranial dysplasia—A case report of incidentally found and lately diagnosed disorder;Clinical Case Reports;2022-10

4. METTL5 regulates cranial suture fusion via Wnt signaling;Fundamental Research;2022-04

5. Genome sequencing identified a novel exonic microdeletion in the RUNX2 gene that causes cleidocranial dysplasia;Clinica Chimica Acta;2022-03