Cleidocranial dysplasia and novel RUNX2 variants: dental, craniofacial, and osseous manifestations
Author:
Affiliation:
1. Chulalongkorn University, Thailand
2. Chiang Mai University, Thailand
3. Chulalongkorn University, Thailand; King Chulalongkorn Memorial Hospital, Thailand
Publisher
FapUNIFESP (SciELO)
Subject
General Dentistry
Link
http://www.scielo.br/scielo.php?script=sci_pdf&pid=S1678-77572022000100426&tlng=en
Reference39 articles.
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2. GeneReviews®;Machol K,2006
3. Cleidocranial dysplasia: molecular genetic analysis and phenotypic-based description of a Middle European patient group;Baumert U;Am J Med Genet A,2005
4. Scheuthauer-Marie-Sainton syndrome;Kuruvila VE;Contemp Clin Dent,2012
5. Cleidocranial dysplasia: a review of clinical, radiological, genetic implications and a guidelines proposal;Farrow E;J Craniofac Surg,2018
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