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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 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.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.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.The Journal of Pathology|July 15, 2006
Epithelial and connective tissue cell CTGF/CCN2 expression in gingival fibrosisA Kantarci, S A Black, C E Xydas, et al.Journal of Medical Genetics|January 11, 2000
Identification of cathepsin C mutations in ethnically diverse papillon-Lefèvre syndrome patientsP S Hart, Y Zhang, E Firatli, et al.Pageof 4