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Publications by Louise Brueton

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

English

Neuropathy in a Human Without the PMP22 Gene

Archives of Neurology

English

Related publications

CBCT Findings in Cleidocranial Dysplasia

Scholars Journal of Dental Sciences

English

Diagnosis of Cleidocranial Dysplasia in Routine Chest Radiograph

Cardiovascular Medicine

English

Cleidocranial Dysplasia Accompanied With Pseudohypoparathyroidism I: Case Report.

Japanese Journal of Oral & Maxillofacial Surgery

English

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

The Journal of Bone and Joint Surgery. British volume

English

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

American Journal of Human Genetics

English

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

Frontiers in Genetics

Molecular Medicine

English

Parietal Foramina With Cleidocranial Dysplasia Is Caused by Mutation in MSX2

European Journal of Human Genetics

English

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

International Journal of Current Microbiology and Applied Sciences

English

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

International Journal of Oral and Maxillofacial Surgery

Otorhinolaryngology

English