-
1
-
-
0024117250
-
Amelogenesis imperfecta, dentinogenesis imperfecta and dentin dysplasia revisited: Problems in classification
-
Witkop CJ. Amelogenesis imperfecta, dentinogenesis imperfecta and dentin dysplasia revisited: problems in classification. J Oral Pathol 1988 17 : 547 553.
-
(1988)
J Oral Pathol
, vol.17
, pp. 547-553
-
-
Witkop, C.J.1
-
2
-
-
0015400959
-
The tricho-dento-osseous (TDO) syndrome
-
Lichtenstein J, Warson R, Jorgenson R, Dorst JP, McKusick VA. The tricho-dento-osseous (TDO) syndrome. Am J Hum Genet 1972 24 : 569 582.
-
(1972)
Am J Hum Genet
, vol.24
, pp. 569-582
-
-
Lichtenstein, J.1
Warson, R.2
Jorgenson, R.3
Dorst, J.P.4
McKusick, V.A.5
-
3
-
-
0027654061
-
Trichodentoosseous (TDO) syndrome: Case report and literature review
-
Seow WK. Trichodentoosseous (TDO) syndrome: case report and literature review. Pediatr Dent 1993 15 : 355 361.
-
(1993)
Pediatr Dent
, vol.15
, pp. 355-361
-
-
Seow, W.K.1
-
5
-
-
0030855974
-
Analysis of the tricho-dento-osseous syndrome genotype and phenotype
-
Wright JT, Kula K, Hall K, Simmons JH, Hart TC. Analysis of the tricho-dento-osseous syndrome genotype and phenotype. Am J Med Genet 1997 72 : 197 204.
-
(1997)
Am J Med Genet
, vol.72
, pp. 197-204
-
-
Wright, J.T.1
Kula, K.2
Hall, K.3
Simmons, J.H.4
Hart, T.C.5
-
6
-
-
0032872958
-
Tricho-dento-osseous syndrome and amelogenesis imperfecta with taurodontism are genetically distinct conditions
-
Price JA, Wright JT, Walker SJ, Crawford PJ, Aldred MJ, Hart TC. Tricho-dento-osseous syndrome and amelogenesis imperfecta with taurodontism are genetically distinct conditions. Clin Genet 1999 56 : 35 40.
-
(1999)
Clin Genet
, vol.56
, pp. 35-40
-
-
Price, J.A.1
Wright, J.T.2
Walker, S.J.3
Crawford, P.J.4
Aldred, M.J.5
Hart, T.C.6
-
7
-
-
0031912018
-
Identification of a mutation in DLX3 associated with tricho-dento-osseous (TDO) syndrome
-
Price JA, Bowden DW, Wright JT, Pettenati MJ, Hart TC. Identification of a mutation in DLX3 associated with tricho-dento-osseous (TDO) syndrome. Hum Mol Genet 1998 7 : 563 569.
-
(1998)
Hum Mol Genet
, vol.7
, pp. 563-569
-
-
Price, J.A.1
Bowden, D.W.2
Wright, J.T.3
Pettenati, M.J.4
Hart, T.C.5
-
8
-
-
18844463423
-
Amelogenesis imperfecta: Autosomal dominant hypomaturation-hypoplasia type with taurodontism
-
Crawford PJM, Evans RD, Aldred MJ. Amelogenesis imperfecta: autosomal dominant hypomaturation-hypoplasia type with taurodontism. Br Dent J 1988 164 : 71 73.
-
(1988)
Br Dent J
, vol.164
, pp. 71-73
-
-
Crawford, P.J.M.1
Evans, R.D.2
Aldred, M.J.3
-
9
-
-
0027202459
-
Taurodontism of the mandibular first permanent molar distinguishes between the tricho-dento-osseous (TDO) syndrome and amelogenesis imperfecta
-
Seow WK. Taurodontism of the mandibular first permanent molar distinguishes between the tricho-dento-osseous (TDO) syndrome and amelogenesis imperfecta. Clin Genet 1993 43 : 240 246.
-
(1993)
Clin Genet
, vol.43
, pp. 240-246
-
-
Seow, W.K.1
-
10
-
-
0025288470
-
Amelogenesis imperfecta with taurodontism and the tricho-dento-osseous syndrome: Separate condition or a spectrum of disease?
-
Crawford PJM, Aldred MJ. Amelogenesis imperfecta with taurodontism and the tricho-dento-osseous syndrome: separate condition or a spectrum of disease? Clin Genet 1990 38 : 44 50.
-
(1990)
Clin Genet
, vol.38
, pp. 44-50
-
-
Crawford, P.J.M.1
Aldred, M.J.2
-
11
-
-
14044252167
-
DLX3 mutation associated with autosomal dominant amelogenesis imperfecta with taurodontism
-
Dong J, Amor D, Aldred MJ, Gu T, Escamilla M, MacDougall M. DLX3 mutation associated with autosomal dominant amelogenesis imperfecta with taurodontism. Am J Med Genet 2005 133 : 138 141.
-
(2005)
Am J Med Genet
, vol.133
, pp. 138-141
-
-
Dong, J.1
Amor, D.2
Aldred, M.J.3
Gu, T.4
Escamilla, M.5
MacDougall, M.6
-
12
-
-
34250157642
-
Tricho-dento-osseous syndrome
-
In: Bergsma, D. (ed.). London: MacMillan
-
Witkop CJ, Worth HM. Tricho-dento-osseous syndrome. In : Bergsma D (ed.). Birth Defects Compendium, 2nd edn. London : MacMillan, 1979 : 1041.
-
(1979)
Birth Defects Compendium, 2nd Edn.
, pp. 1041
-
-
Witkop, C.J.1
Worth, H.M.2
-
13
-
-
0030455359
-
Craniofacial morphology of the tricho-dento-osseous syndrome
-
Kula K, Hall K, Hart T, Wright JT. Craniofacial morphology of the tricho-dento-osseous syndrome. Clin Genet 1996 50 : 446 454.
-
(1996)
Clin Genet
, vol.50
, pp. 446-454
-
-
Kula, K.1
Hall, K.2
Hart, T.3
Wright, J.T.4
-
14
-
-
17744409669
-
Enamel structure and composition in the tricho-dento-osseous syndrome
-
Spangler GS, Hall KI, Kula K, Hart TC, Wright JT. Enamel structure and composition in the tricho-dento-osseous syndrome. Connect Tissue Res 1998 39 : 165 175.
-
(1998)
Connect Tissue Res
, vol.39
, pp. 165-175
-
-
Spangler, G.S.1
Hall, K.I.2
Kula, K.3
Hart, T.C.4
Wright, J.T.5
-
15
-
-
0030728173
-
Genetic linkage of the tricho-dento-osseous syndrome to chromosome 17q21
-
Hart TC, Bowden DW, Bolyard J, Kula K, Hall K, Wright JT. Genetic linkage of the tricho-dento-osseous syndrome to chromosome 17q21. Hum Mol Genet 1997 6 : 2279 2284.
-
(1997)
Hum Mol Genet
, vol.6
, pp. 2279-2284
-
-
Hart, T.C.1
Bowden, D.W.2
Bolyard, J.3
Kula, K.4
Hall, K.5
Wright, J.T.6
-
16
-
-
27944484434
-
Clinical features of tricho-dento-osseous syndrome and presentation of three new cases: An addition to clinical heterogeneity
-
Islam M, Lurie AG, Reichenberger E. Clinical features of tricho-dento-osseous syndrome and presentation of three new cases: an addition to clinical heterogeneity. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 2005 100 : 736 742.
-
(2005)
Oral Surg Oral Med Oral Pathol Oral Radiol Endod
, vol.100
, pp. 736-742
-
-
Islam, M.1
Lurie, A.G.2
Reichenberger, E.3
-
18
-
-
0020545018
-
Clinical heterogeneity in the tricho-dento-osseous syndrome
-
Quattromani F, Shapiro SD, Young RS, et al. Clinical heterogeneity in the tricho-dento-osseous syndrome. Hum Genet 1983 64 : 116 121.
-
(1983)
Hum Genet
, vol.64
, pp. 116-121
-
-
Quattromani, F.1
Shapiro, S.D.2
Young, R.S.3
-
19
-
-
5344238900
-
Increased bone density associated with DLX3 mutation in the tricho-dento-osseous syndrome
-
Haldeman RJ, Cooper LF, Hart TC, et al. Increased bone density associated with DLX3 mutation in the tricho-dento-osseous syndrome. Bone 2004 35 : 988 997.
-
(2004)
Bone
, vol.35
, pp. 988-997
-
-
Haldeman, R.J.1
Cooper, L.F.2
Hart, T.C.3
-
20
-
-
9144248989
-
Novel ENAM mutation responsible for autosomal recessive amelogenesis imperfecta and localised enamel defects
-
Hart TC, Hart PS, Gorry MC, et al. Novel ENAM mutation responsible for autosomal recessive amelogenesis imperfecta and localised enamel defects. J Med Genet 2003 40 : 900 906.
-
(2003)
J Med Genet
, vol.40
, pp. 900-906
-
-
Hart, T.C.1
Hart, P.S.2
Gorry, M.C.3
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