Progressive cognitive decline in an adult patient with cleidocranial dysplasia
Author:
Publisher
Elsevier BV
Subject
Genetics(clinical),Genetics,General Medicine
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4. Cleidocranial dysplasia plus vascular anomalies with 6p21.2 microdeletion spanning RUNX2 and VEGF;Izumi;Am J Med Genet A,2006
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3. A Novel 90-kbp Deletion of RUNX2 Associated with Cleidocranial Dysplasia;Genes;2022-06-23
4. Genome sequencing identified a novel exonic microdeletion in the RUNX2 gene that causes cleidocranial dysplasia;Clinica Chimica Acta;2022-03
5. Genetic Pattern, Orthodontic and Surgical Management of Multiple Supplementary Impacted Teeth in a Rare, Cleidocranial Dysplasia Patient: A Case Report;Medicina;2021-12-10
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