Deletions of the RUNX2 Gene Are Present in About 10% of Individuals With Cleidocranial Dysplasia

Human Mutation - United States
doi 10.1002/humu.21298
Full Text
Abstract

Available in full text

Categories
Genetics
Date
Authors
Publisher

Wiley

Related search

CBCT Findings in Cleidocranial Dysplasia

Scholars Journal of Dental Sciences
2020English

Diagnosis of Cleidocranial Dysplasia in Routine Chest Radiograph

Circulation
Cardiovascular MedicinePhysiologyCardiology
2007English

Cleidocranial Dysplasia Accompanied With Pseudohypoparathyroidism I: Case Report.

Japanese Journal of Oral & Maxillofacial Surgery
1989English

The ‘Chef’s Hat’ Appearance of the Femoral Head in Cleidocranial Dysplasia

The Journal of Bone and Joint Surgery. British volume
2000English

Mutation Analysis of Core Binding Factor A1 in Patients With Cleidocranial Dysplasia

American Journal of Human Genetics
Genetics
1999English

Gene-Expression Analysis Identifies IGFBP2 Dysregulation in Dental Pulp Cells From Human Cleidocranial Dysplasia

Frontiers in Genetics
GeneticsMolecular Medicine
2018English

Parietal Foramina With Cleidocranial Dysplasia Is Caused by Mutation in MSX2

European Journal of Human Genetics
Genetics
2003English

Molecular Characterization of Cleidocranial Dysplasia (CCD) in the Western Region in KSA

International Journal of Current Microbiology and Applied Sciences
2017English

Abnormal Ossification of the Hyoid Bone in Cleidocranial Dysplasia Rare Case and Literature Review

International Journal of Oral and Maxillofacial Surgery
OtorhinolaryngologyOral SurgerySurgery
2017English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2025 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy