Surgical Management and Evaluation of the Craniofacial Growth and Morphology in Cleidocranial Dysplasia-Reference-Cited by-同舟云学术

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Surgical Management and Evaluation of the Craniofacial Growth and Morphology in Cleidocranial Dysplasia

Published:2018-06 Issue:4 Volume:29 Page:959-965
ISSN:1049-2275
Container-title:Journal of Craniofacial Surgery
language:en
Short-container-title:Journal of Craniofacial Surgery

Author:

Greene Stephen L.,Kau Chung How,Sittitavornwong Somsak,Powell Kathlyn,Childers Noel K.,MacDougall Mary,Lamani Ejvis

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

General Medicine,Otorhinolaryngology,Surgery

Reference33 articles.

1. Genetic mapping of cleidocranial dysplasia and evidence of a microdeletion in one family

2. Missense mutations abolishing DNA binding of the osteoblast-specific transcription factor OSF2/CBFA1 in cleidocranial dysplasia

3. Mutations Involving the Transcription Factor CBFA1 Cause Cleidocranial Dysplasia

4. Mutations in theRUNX2 gene in patients with cleidocranial dysplasia

5. Runx2 Regulates Endochondral Ossification Through Control of Chondrocyte Proliferation and Differentiation

Cited by 11 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. CLINICAL CASE OF CRANIOCLAVICAL DYSOSTOSIS SYNDROME: CLINICAL AND X-RAY MANIFESTATIONS;Actual problems in dentistry;2023-11-30

2. The Benefits of CBCT Imaging in the Diagnosis of Individuals with Craniofacial Anomalies;Journal of the California Dental Association;2023-08-24

3. A novel single‐base deletion of the RUNX Family Transcription Factor 2 gene associated with cleidocranial dysplasia;European Journal of Oral Sciences;2023-01-04

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

5. Multiplanar imaging in a familial case of cleidocranial dysplasia and various orthodontic-surgical protocols approved for its treatment;Hamdan Medical Journal;2022

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