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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.
  • 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
  • 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
  • 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
  • 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
  • 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
  • 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
  • 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
  • 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

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  • 1张慧,陈柯.遗传性乳光牙本质1例[J].牙体牙髓牙周病学杂志,2005,15(6):360-360. 被引量:1
  • 2侯燕宁,崔英霞.一例牙本质发育不全Ⅱ型家系报告[J].中国优生与遗传杂志,2005,13(10):101-101. 被引量:1
  • 3杨帆,陆瑛,俞萍,赵士芳.遗传性牙本质发育不全Ⅱ型DSPP基因新突变[J].口腔医学,2006,26(3):226-228. 被引量:6
  • 4赵高峰,黄向东,汪昌宁,宋亚玲,边专.牙本质发育异常家系调查和表型分析[J].口腔医学研究,2006,22(4):444-447. 被引量:2
  • 5王巧云,王秀玉,江庆,王潇,王毅,梁其彬.牙本质发育不全Ⅲ型——壳牙1例[J].实用口腔医学杂志,2006,22(6):745-745. 被引量:2
  • 6Malmgren B, Lindskog S, Elgadi A, et al. Clinical, histopathologic and genetic investigation in two large families with dentinogenesis impefecta type II[ J ]. Hum Genet, 2004, 114(5) :491 -498.
  • 7Aplin HM, Hirst KL, Dixon MJ. Refinement of the dentinogenesis imperfecta type II locus to an interval of less than 2 centiMorgarm at chromosome 4q21 and the creation of a yeast artificial chromosome contig of the critical region[ J]. J Dent Res, 1999, 78(6) :1270 -1276.
  • 8Witkop CJ. Medical and dental findings in the Brandywine isolation [J]. AL J Med Sci, 1966, 3:382.
  • 9Zhang Xiaohai, Zhao Jun, Li Changfu, et al. DSPP mutation in dentinogenesis imperfecta Shields type II [ J ]. Nat Genet, 2001, 27(2):151-152.
  • 10Kim JW, Nam SH, Jang KT, et al. A novel splice acceptor mutation in the DSPP gene causing dentinagenesis imperfecta type II [J]. Hum Genet, 2004, 115(3) : 248 - 254.

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