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牙本质发育不全1例 被引量:1

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出处 《现代口腔医学杂志》 CAS CSCD 北大核心 2008年第2期201-201,共1页 Journal of Modern Stomatology
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  • 1赵军 冯毅.遗传性乳光牙本质一家系[J].中华医学遗传学杂志,1999,16:43-43. 被引量:1
  • 2Shields ED, Bixler D, E1 - Kafrawy AM. A proposed classification for heritable human dentine defect with a description of a new entity [J]. Arch Oral Biol, 1973,18(4):543 -553 被引量:1
  • 3Dean JA, Hartsfield JK Jr, Wright JT, et al. Dentin dysplasia,type II linkage to chromosome 4q [J]. J Craniofac Gene. Dev Biol, 1997, 17(4): 172-177 被引量:1
  • 4Xiao S, Yu C, Chou X, et al. Dentinogenesis imperfecta 1 with or without progressive hearing loss is associated with distinct mutations in DSPP [ J ]. Nature Genet, 2001, 27 ( 2 ) : 201 - 204 被引量:1
  • 5MacDougall M, Jeffords LG, Gu TT, et al. Genetic linkage of the dentinogenesis imperfecta type Ⅲ locus to chromosome 4q [ J]. J Dent Res, 1999, 78(6): 1 277- 1 282 被引量:1
  • 6Rajpar MH, Koch MJ, Davies RM, et al. Mutation of the signal peptide region of the bicistronic gene DSPP affects translocation to the endoplasmic reticulum and results in defective dentine biomineralization [ J ]. Hum Molec Genet, 2002, 11 ( 21 ) : 2 559 - 2 565 被引量:1
  • 7Levin LS, Leaf SH, Jelmini R J, et al. Dentinogenesis imperfecta in the Brandywine isolate (DI type Ⅲ): clinical, radiologic, and scanning electron microscopic studies of the dentition [ J ]. Oral Surg Oral Med Oral Path, 1983, 56(3):267 -274 被引量:1
  • 8Kim J - W, Hu JC - C, Lee J - I1, et al. Mutational hot spot in the DSPP gene causing dentinogenesis imperfecta type Ⅱ[ J ].Hum Genet, 2005, 116(3): 186 -191 被引量:1
  • 9Dong J, Gu TT, Jeffords L, et al. Dentin phosphoprotein compound mutation in dentin sialophosphoprotein causes dentinogenesis imperfecta type III [J]. Am J Med Genet A, 2005, 132(3):305 - 309 被引量:1

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