Foreword to volume 3, issue 6

Por Hart, P. Suzanne, Muenke, Maximilian
Publicado no Mol Genet Genomic Med (2015)

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)

Hereditary Interstitial Kidney Disease

Por Bleyer, Anthony J., Hart, P. Suzanne, Kmoch, Stanislav
Publicado no Semin Nephrol (2010)

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)

Medical genetics and genomic medicine in the United States of America. Part 1: history, demographics, legislation, and burden of disease

Por Ferreira, Carlos R., Regier, Debra S., Hadley, Donald W., Hart, P. Suzanne, Muenke, Maximilian
Publicado no Mol Genet Genomic Med (2017)

Childhood course of renal insufficiency in a family with a uromodulin gene mutation

Por Schäffer, Péter, Gombos, Éva, Meichelbeck, Krisztina, Kiss, András, Hart, P. Suzanne, Bleyer, Anthony J.
Publicado no Pediatr Nephrol (2010)

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)

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

Amelogenesis Imperfecta: Genotype-Phenotype Studies in 71 Families

Por Wright, J. Timothy, Torain, Melody, Long, Kimberly, Seow, Kim, Crawford, Peter, Aldred, Michael J., Hart, P. Suzanne, Hart, Tom C.
Publicado em 2011

A comprehensive analysis of normal variation and disease-causing mutations in the human DSPP gene

Por McKnight, Dianalee A., Hart, P. Suzanne, Hart, Thomas C., Hartsfield, James K., Wilson, Anne, Wright, J. Timothy, Fisher, Larry W.
Publicado no Hum Mutat (2008)

Noncompaction of the Ventricular Myocardium and Hydrops Fetalis in Cobalamin C Disease

Por Tanpaiboon, Pranoot, Sloan, Jennifer L., Callahan, Patrick F., McAreavey, Dorothea, Hart, P. Suzanne, Lichter-Konecki, Uta, Zand, Dina, Venditti, Charles P.
Publicado em 2012

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

Identification of 2 Novel ANTXR2 Mutations in Patients With Hyaline Fibromatosis Syndrome and Proposal of a Modified Grading System

Por Denadai, Rafael, Raposo-Amaral, Cassio E., Bertola, Débora, Kim, Chong, Alonso, Nivaldo, Hart, Thomas, Han, Sangwoo, Stelini, Rafael F., Buzzo, Celso L., Raposo-Amaral, Cesar A., Hart, P. Suzanne
Publicado no Am J Med Genet A (2012)

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

Chediak-Higashi Syndrome with early Developmental Delay resulting from Paternal Heterodisomy of Chromosome 1

Por Manoli, Irini, Golas, Gretchen, Westbroek, Wendy, Vilboux, Thierry, Markello, Thomas C., Introne, Wendy, Maynard, Dawn, Pederson, Ben, Tsilou, Ekaterini, Jordan, Michael B., Hart, P. Suzanne, White, James G., Gahl, William A., Huizing, Marjan
Publicado em 2010

The PDGF-C regulatory region SNP rs28999109 decreases promoter transcriptional activity and is associated with CL/P

Por Choi, Sun J, Marazita, Mary L, Hart, P Suzanne, Sulima, Pawel P, Field, L Leigh, McHenry, Toby Goldstein, Govil, Manika, Cooper, Margaret E, Letra, Ariadne, Menezes, Renato, Narayanan, Somnya, Mansilla, Maria Adela, Granjeiro, José M, Vieira, Alexandre R, Lidral, Andrew C, Murray, Jeffrey C, Hart, Thomas C
Publicado em 2009

Dominant Renin Gene Mutations Associated with Early-Onset Hyperuricemia, Anemia, and Chronic Kidney Failure

Por Živná, Martina, Hůlková, Helena, Matignon, Marie, Hodaňová, Kateřina, Vylet'al, Petr, Kalbáčová, Marie, Barešová, Veronika, Sikora, Jakub, Blažková, Hana, Živný, Jan, Ivánek, Robert, Stránecký, Viktor, Sovová, Jana, Claes, Kathleen, Lerut, Evelyne, Fryns, Jean-Pierre, Hart, P. Suzanne, Hart, Thomas C., Adams, Jeremy N., Pawtowski, Audrey, Clemessy, Maud, Gasc, Jean-Marie, Gübler, Marie-Claire, Antignac, Corinne, Elleder, Milan, Kapp, Katja, Grimbert, Philippe, Bleyer, Anthony J., Kmoch, Stanislav
Publicado em 2009