1 |
Kim JW, Simmer JP. Hereditary dentin defects[J]. J Dent Res, 2007, 86(5): 392-399.
|
2 |
Barron MJ, McDonnell ST, Mackie I, et al. Hereditary dentine disorders: dentinogenesis imperfecta and dentine dysplasia[J]. Orphanet J Rare Dis, 2008, 3: 31.
|
3 |
McKnight DA, Simmer JP, Hart PS, et al. Overlapping DSPP mutations cause dentin dysplasia and dentinogenesis imperfecta[J]. J Dent Res, 2008, 87(12): 1108-1111.
|
4 |
Bloch-Zupan A, Jamet X, Etard C, et al. Homozygosity mapping and candidate prioritization identify mutations, missed by whole-exome sequencing, in SMOC2, cau-sing major dental developmental defects[J]. Am J Hum Genet, 2011, 89(6): 773-781.
|
5 |
Yang Q, Chen D, Xiong F, et al. A splicing mutation in VPS4B causes dentin dysplasiaⅠ[J]. J Med Genet, 2016, 53(9): 624-633.
|
6 |
Xiong F, Ji Z, Liu Y, et al. Mutation in SSUH2 causes autosomal-dominant dentin dysplasia type Ⅰ[J]. Hum Mutat, 2017, 38(1): 95-104.
|
7 |
Gu Y, Tang Y, Zhu Q, et al. Measurement of root surface area of permanent teeth with root variations in a Chinese population-A micro-CT analysis[J]. Arch Oral Biol, 2016, 63: 75-81.
|
8 |
Versiani MA, Carvalho KKT, Mazzi-Chaves JF, et al. Micro-computed tomographic evaluation of the shaping ability of XP-endo Shaper, iRaCe, and EdgeFile Systems in long oval-shaped canals[J]. J Endod, 2018, 44(3): 489-495.
|
9 |
杨梅, 贾杰, 宋亚玲. 牙本质发育不全表型分析及突变筛查[J]. 口腔生物医学, 2017, 8(1): 11-15.
|
|
Yang M, Jia J, Song YL. Phenotype analysis and mutation screening on dentinogenesis imperfecta[J]. Oral Bio-med, 2017, 8(1): 11-15.
|
10 |
Ye X, Li K, Liu L, et al. Dentin dysplasia type Ⅰ-novel findings in deciduous and permanent teeth[J]. BMC Oral Health, 2015, 15: 163.
|
11 |
Taleb K, Lauridsen E, Daugaard-Jensen J, et al. Dentinogenesis imperfecta type Ⅱ-genotype and phenotype analyses in three Danish families[J]. Mol Genet Genomic Med, 2018, 6(3): 339-349.
|
12 |
Kühnisch J, Galler M, Seitz M, et al. Irregularities below the enamel-dentin junction may predispose for fissure caries[J]. J Dent Res, 2012, 91(11): 1066-1070.
|
13 |
Farah RA, Swain MV, Drummond BK, et al. Mineral density of hypomineralised enamel[J]. J Dent, 2010, 38(1): 50-58.
|
14 |
Zhang X, Rahemtulla F, Zhang P, et al. Normalisation of calcium status reverses the phenotype in dentin, but not in enamel of VDR-deficient mice[J]. Arch Oral Biol, 2009, 54(12): 1105-1110.
|
15 |
Davis GR, Fearne JM, Sabel N, et al. Microscopic study of dental hard tissues in primary teeth with Dentinogenesis Imperfecta Type Ⅱ: correlation of 3D imaging using X-ray microtomography and polarising microscopy[J]. Arch Oral Biol, 2015, 60(7): 1013-1020.
|
16 |
Olejniczak AJ, Smith TM, Feeney RN, et al. Dental tissue proportions and enamel thickness in Neandertal and modern human molars[J]. J Hum Evol, 2008, 55(1): 12-23.
|
17 |
王书明, 张大鹏, 郑亚琪, 等. 人下颌第一磨牙釉质帽与牙本质核三维形态的初步研究[J]. 牙体牙髓牙周病学杂志, 2014(12): 705-708, 728.
|
|
Wang SM, Zhang DP, Zheng YQ, et al. A preliminary 3-dimensional study of the enamel cap and dentin core of human mandibular first molar[J]. Chin J Conservat Dent, 2014(12): 705-708, 728.
|
18 |
Turkkahraman H, Galindo F, Tulu US, et al. A novel hypothesis based on clinical, radiological, and histological data to explain the dentinogenesis imperfecta typeⅡphenotype[J]. Connect Tissue Res, 2020, 61(6): 526-536.
|
19 |
Carroll MKO, Duncan WK, Perkins TM. Dentin dysplasia: review of the literature and a proposed subclassification based on radiographic findings[J]. Oral Surg Oral Med Oral Pathol, 1991, 72(1): 119-125.
|
20 |
Wright T. The molecular control of and clinical variations in root formation[J]. Cells Tissues Organs, 2007, 186(1): 86-93.
|