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Case Reports in Dentistry|January 15, 2015
Craniodentofacial Manifestations in a Rare Syndrome: Orofaciodigital Type IV (Mohr-Majewski Syndrome)Meltem Ozdemir-Karatas, Didem Ozdemir-Ozenen, P Suzanne Hart, et al.Pediatric Dentistry|January 30, 2010
Oral rehabilitation of a patient with amelogenesis imperfectaDilsah Cogulu, Sema Becerik, Gülnur Emingil, et al.Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontics|February 19, 2004
Phenotypic diversity and revision of the nomenclature for autosomal recessive amelogenesis imperfectaMohamad Nusier, Othman Yassin, Thomas C Hart, et al.American Journal of Medical Genetics. Part A|September 27, 2006
Craniofacial and dental phenotype of Smith-Magenis syndromeNatalia Tomona, Ann C M Smith, Jean Pierre Guadagnini, et al.Journal of Dentistry for Children (Chicago, Ill.)|April 3, 2010
Novel cathepsin C mutation in a Brazilian family with Papillon-Lefèvre syndrome: case report and mutation updateDebora Pallos, Ana Carolina Acevedo, Heliana Dantas Mestrinho, et al.Kidney International|August 26, 2004
Mutations in the uromodulin gene decrease urinary excretion of Tamm-Horsfall proteinAnthony J Bleyer, Thomas C Hart, Zak Shihabi, et al.Journal of Dental Education|June 7, 2013
The utility of hybrid promotion and tenure tracks for dental school facultyBernard J Costello, Kathy L Marshall, Tara Schafer, et al.American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|August 6, 2003
Renal manifestations of a mutation in the uromodulin (Tamm Horsfall protein) geneAnthony J Bleyer, Howard Trachtman, Jaspreet Sandhu, et al.Journal of Periodontology|November 1, 2013
Proteomic analyses of human gingival and periodontal ligament fibroblastsHolly McKnight, W Patrick Kelsey, Deborah A Hooper, et al.American Journal of Medical Genetics. Part A|June 17, 2009
Exclusion of candidate genes in seven Turkish families with autosomal recessive amelogenesis imperfectaSema Becerik, Dilsah Cogulu, Gülnur Emingil, et al.Pageof 8