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T.C. Hart

Human Craniofacial Genetics Section

Skeletal and Craniofacial Diseases Branch

National Institute of Dental and Craniofacial Research

National Institutes of Health



Name/email consistency: high



  • Human Craniofacial Genetics Section, Skeletal and Craniofacial Diseases Branch, National Institute of Dental and Craniofacial Research, National Institutes of Health, USA. 2009
  • Department of Oral Medicine and Pathology, School of Dental Medicine, University of Pittsburgh, Pittsburgh, USA. 2003


  1. Genetic studies of craniofacial anomalies: clinical implications and applications. Hart, T.C., Hart, P.S. Orthod. Craniofac. Res (2009) [Pubmed]
  2. Novel ENAM mutation responsible for autosomal recessive amelogenesis imperfecta and localised enamel defects. Hart, T.C., Hart, P.S., Gorry, M.C., Michalec, M.D., Ryu, O.H., Uygur, C., Ozdemir, D., Firatli, S., Aren, G., Firatli, E. J. Med. Genet. (2003) [Pubmed]
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