Amelogenesis Imperfecta
Dentinogenesis Imperfect
Tricho Dento Osseous
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References

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51. MacDougall M, Jeffords LG, Gu TT, Knight CB, Frei G, Reus BE, Otterud B, Leppert M. Genetic linkage of the dentinogenesis imperfecta type III locus to chromsome 4q. J Dent Res 1999;78:1277-1282.

52. Xiao S, Yu C, Chou X, Yuan W, Wang Y, Bu L, Fu G, Qian M, Yang J, Shi Y, Hu L, Han B, Wang Z, Huang W, Liu J, Chen Z, Zhao G, Kong X. Dentinogenesis imperfecta 1 with or without progressive hearing loss is associated with distinct mutations in DSPP. Nat Genet 2001;27:201-204.

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60. Pashley DH. Dynamics of the pulpo-dentin complex. Crit Rev Oral Biol Med 1996;7:104-133.

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63. Kim JW, Lee SK, Lee ZH, Park JC, Lee KE, Lee MH, et al., FAM83H mutations in families with autosomal-dominant hypocalcified amelogenesis imperfecta. Am J Hum Genet, 2008. 82: 489-94.

64.Hart PS, Becerik S, Cogulu D, Emingil G, Ozdemir-Ozenen D, Han ST, et al., Novel FAM83H mutations in Turkish families with autosomal dominant hypocalcified amelogenesis imperfecta. Clin Genet, 2009. 75: 401-4.

65.Wright JT, Frazier-Bowers S, Simmons D, Alexander K, Crawford P, Han ST, et al., Phenotypic variation in FAM83H-associated amelogenesis imperfecta. J Dent Res, 2009. 88: 356-60.

66.Lee SK, Hu JC, Bartlett JD, Lee KE, Lin BP, Simmer JP, et al., Mutational spectrum of FAM83H: the C-terminal portion is required for tooth enamel calcification. Hum Mutat, 2008.

67.Wright JT, Deaton TC, Hall KI, Yamauchi M, The mineral and protein content of enamel in amelogenesis imperfecta. Connect Tissue Res, 1995. 31: 247-252.

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