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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

USA

[email]@mail.nih.gov

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Affiliations

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

References

Genetic studies of craniofacial anomalies: clinical implications and applications. Hart, T.C., Hart, P.S. Orthod. Craniofac. Res (2009) [Pubmed]
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]