Browsing by Author Hart, Thomas Charles

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Showing results 1 to 15 of 15
Issue DateTitleAuthor(s)Type
1998Genetic linkage of hereditary gingival fibromatosis to chromosome 2p21-Artigo de Periódico
1999[DUPLICADO} Genetic heterogeneity of gingival fibromatosis on chromosome 2p-Artigo de Periódico
1999[DUPLICADO] Genetic heterogeneity of gingival fibromatosis on chromosome 2p-Artigo de Periódico
2000Evidence of genetic heterogeneity for hereditary gingival fibromatosis-Artigo de Periódico
1997Altered post-translational modifications of collagen in hereditary gingival fibromatosis.-Resumo
1998Evidence for genetic heterogeneity for hereditary gingival fibromatosis.-Resumo
1998Localization of a hereditary gingival fibromatosis gene to chromosome 2p.-Resumo
2001Novel COL1A1 mutation (G599C) associated with mild osteogenesis imperfecta and dentinogenesis imperfecta-Artigo de Periódico
2003Evaluation of human leukocyte N-formylpeptide receptor (FPR1) SNPs in aggressive periodontitis patients-Artigo de Periódico
2000Novel COL1A1 mutation (G599C) associated with mild osteogenesis imperfecta and dentinogenesis imperfecta.-Resumo
1997Prevalence of gingival recession in young Brazilian individuals.-Resumo
1996Genetic studies of hereditary gingival fibromatosis-Resumo
2007Germ line gain of function with SOS1 mutation in hereditary gingival fibromatosis-Artigo de Periódico
2010Novel cathepsin C mutation in a Brazilian family with Papillon- Lefèvre syndrome: Case report and mutation update-Artigo de Periódico
2006Characterization of fibroblasts with Son of Sevenless-1 mutation-Artigo de Periódico