Scientific research direction

Craniofacial development and Hereditary diseases Domain

Increasing the understanding of molecular basis of human hereditary and developmental malformations:
Database collection of home system and samples of craniofacial hereditary diseases. 
Molecular mechanism of teeth, bone and soft tissue development in oral and maxillofacial 
Pathogenetic mechanisms, prevention and early intervention therapy of causative mutations, signaling pathways involved in normal and abnormal developmental processes, and phenotype-genotype correlations.