D4S35 and D4S103 identify the same locus and MspI RFLP

Por Hart, Thomas C., Diehl, Scott R.
Publicado em 1990

Disorders of Human Dentin

Por Hart, P. Suzanne, Hart, Thomas C.
Publicado no Cells Tissues Organs (2007)

Invited commentary: The need for human genetics and genomics in dental school curricula

Por Hart, P. Suzanne, Hart, Thomas C.
Publicado no Mol Genet Genomic Med (2016)

Evidence of a contribution of genetic factors to dental caries risk

Por Bretz, Walter A., Corby, Patricia, Schork, Nicholas, Hart, Thomas C.
Publicado em 2003

Oral Rehabilitation of a Patient with Amelogenesis Imperfecta

Por Cogulu, Dilsah, Becerik, Sema, Emingil, Gülnur, Hart, P. Suzanne, Hart, Thomas C.
Publicado no Pediatr Dent (2009)

Craniodentofacial Manifestations in a Rare Syndrome: Orofaciodigital Type IV (Mohr-Majewski Syndrome)

Por Ozdemir-Karatas, Meltem, Ozdemir-Ozenen, Didem, Hart, P. Suzanne, Hart, Thomas C.
Publicado no Case Rep Dent (2014)

Exclusion of Candidate Genes in Seven Turkish Families With Autosomal Recessive Amelogenesis Imperfecta

Por Becerik, Sema, Cogulu, Dilsah, Emingil, Gülnur, Han, Ted, Hart, P. Suzanne, Hart, Thomas C.
Publicado no Am J Med Genet A (2009)

A Unique Form of Mental Retardation with a Distinctive Phenotype Maps to Xq26-q27

Por Shashi, Vandana, Berry, Margaret N., Shoaf, Sarah, Sciote, James J., Goldstein, Donald, Hart, Thomas C.
Publicado em 2000

Novel Cathepsin C Mutation in a Brazilian Family with Papillon-Lefèvre Syndrome: Case Report and Mutation Update

Por Pallos, Debora, Acevedo, Ana Carolina, Mestrinho, Heliana Dantas, Cordeiro, Ilia, Hart, Thomas C., Hart, P. Suzanne
Publicado no J Dent Child (Chic) (2010)

Exclusion of known gene for enamel development in two Brazilian families with amelogenesis imperfecta

Por Santos, Maria CLG, Hart, P Suzanne, Ramaswami, Mukundhan, Kanno, Cláudia M, Hart, Thomas C, Line, Sergio RP
Publicado em 2007

A Characterization of the Oral Microbiome in Allogeneic Stem Cell Transplant Patients

Por Ames, Nancy J., Sulima, Pawel, Ngo, Thoi, Barb, Jennifer, Munson, Peter J., Paster, Bruce J., Hart, Thomas C.
Publicado em 2012

Using Biometrics for Participant Identification in a Research Study: a Case Report

Por Corby, Patricia M., Schleyer, Titus, Spallek, Heiko, Hart, Thomas C., Weyant, Robert J., Corby, Andrea L., Bretz, Walter A.
Publicado em 2006

Mutant DLX 3 disrupts odontoblast polarization and dentin formation

Por Choi, S.J., Song, I.S., Feng, J.Q., Gao, T., Haruyama, N., Gautam, P., Robey, P.G., Hart, Thomas C.
Publicado em 2010

Heritability of Oral Microbial Species in Caries-Active and Caries-Free Twins

Por Corby, Patricia M., Bretz, Walter A., Hart, Thomas C., Schork, Nicholas J., Wessel, J, Lyons-Weiler, James, Paster, Bruce J.
Publicado em 2007

A 4 bp deletion mutation in DLX3 enhances osteoblastic differentiation and bone formation in vitro

Por Choi, Sun Jin, Song, In Sun, Ryu, Ok Hee, Choi, Sung Won, Suzanne Hart, P., Wu, Wells W., Shen, Rong-Fong, Hart, Thomas C.
Publicado em 2007

Identification of Microbial and Proteomic Biomarkers in Early Childhood Caries

Por Hart, Thomas C., Corby, Patricia M., Hauskrecht, Milos, Hee Ryu, Ok, Pelikan, Richard, Valko, Michal, Oliveira, Maria B., Hoehn, Gerald T., Bretz, Walter A.
Publicado em 2011

A Mutation in the SOS1 Gene Causes Hereditary Gingival Fibromatosis Type 1

Por Hart, Thomas C., Zhang, Yingze, Gorry, Michael C., Hart, P. Suzanne, Cooper, Margaret, Marazita, Mary L., Marks, Jared M., Cortelli, Jose R., Pallos, Debora
Publicado em 2002

Oral and Dental Phenotype of Dyskeratosis Congenita

Por Atkinson, Jane C., Harvey, Kristen E., Domingo, Demetrio L., Trujillo, Maria I., Guadagnini, Jean-Pierre, Gollins, Sherri, Giri, Neelam, Hart, Thomas C., Alter, Blanche P.
Publicado em 2008

A case of familial tumoral calcinosis/hyperostosis-hyperphosphatemia syndrome due to a compound heterozygous mutation in GALNT3 demonstrating new phenotypic features

Por Dumitrescu, Claudia E., Kelly, Marilyn H., Khosravi, Azarmindokht, Hart, Thomas C., Brahim, Jaime, White, Kenneth E., Farrow, Emily G., Nathan, Muriel H., Murphey, Mark D., Collins, Michael T.
Publicado em 2008

Human and Mouse Enamel Phenotypes Resulting from Mutation or Altered Expression of AMEL, ENAM, MMP20 and KLK4

Por Wright, J. Timothy, Hart, Thomas C., Hart, P. Suzanne, Simmons, Darrin, Suggs, Cynthia, Daley, Bill, Simmer, Jim, Hu, Jan, Bartlett, John D., Li, Yong, Yuan, Zhi-An, Seow, W. Kim, Gibson, Carolyn W.
Publicado em 2008