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Journal of Dental Research|October 26, 2005
Phenotype of ENAM mutations is dosage-dependentD Ozdemir, P S Hart, E Firatli, et al.Journal of Medical Genetics|December 20, 2003
Novel ENAM mutation responsible for autosomal recessive amelogenesis imperfecta and localised enamel defectsT C Hart, P S Hart, M C Gorry, et al.Journal of Dental Research|October 26, 2005
MMP20 active-site mutation in hypomaturation amelogenesis imperfectaD Ozdemir, P S Hart, O H Ryu, et al.Orthodontics & Craniofacial Research|July 25, 2009
Genetic studies of craniofacial anomalies: clinical implications and applicationsT C Hart, P S HartJournal of Medical Genetics|December 14, 1999
Mutations of the cathepsin C gene are responsible for Papillon-Lefèvre syndromeT C Hart, P S Hart, D W Bowden, et al.Journal of Medical Genetics|February 7, 2001
Evidence of a founder effect for four cathepsin C gene mutations in Papillon-Lefèvre syndrome patientsY Zhang, T Lundgren, S Renvert, et al.Genes and Immunity|February 22, 2003
Evaluation of human leukocyte N-formylpeptide receptor (FPR1) SNPs in aggressive periodontitis patientsY Zhang, R Syed, C Uygar, et al.Journal of Medical Genetics|February 9, 2000
Haim-Munk syndrome and Papillon-Lefèvre syndrome are allelic mutations in cathepsin CT C Hart, P S Hart, M D Michalec, et al.Archives of Oral Biology|April 2, 2002
A nomenclature for X-linked amelogenesis imperfectaP S Hart, T C Hart, J P Simmer, et al.Journal of Periodontology|February 1, 1997
The relationship between clinical periodontal status and insulin-dependent diabetes mellitus. Results after 5 yearsE FiratliPageof 19