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See Latest ArticlesNovel RUNX2 Mutations in Chinese Individuals with Cleidocranial Dysplasia
Journal of Dental Research , 09/25/09
Zhang CY et al. – Cleidocranial dysplasia (CCD) is an inherited autosomal–dominant skeletal disease caused by heterozygous mutations in the osteoblast–specific transcription factor, RUNX2. The results provide new genetic evidence that mutations involved in RUNX2 contribute to CCD.
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Today in Basic Science...keeping you current
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De novo mutation in the DSPP gene associated with dentinogenesis imperfecta type II in a Japanese family
European Journal of Oral Sciences, 11/19/09
Upregulation of vimentin and aberrant expression of E-cadherin/beta-catenin complex in oral squamous cell carcinomas: correlation with the clinicopathological features and patient outcome
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Today in Orthodontics/Dentofacial...keeping you current
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Influence of edentulousness on gonial angle, ramus and condylar height
Journal of Oral Rehabilitation, 11/24/09
Cleidocranial dysplasia: A family report
Journal of Indian Society of Pedodontics and Preventive Dentistry , 11/24/09
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