-
1
-
-
16244398032
-
Hypodontia-a retrospective review of prevalence and etiology. Part I
-
Larmour C.J., Mossey P.A., Thind B.S., Forgie A.H., and Stirrups D.R. Hypodontia-a retrospective review of prevalence and etiology. Part I. Quintessence Int 36 (2005) 263-270
-
(2005)
Quintessence Int
, vol.36
, pp. 263-270
-
-
Larmour, C.J.1
Mossey, P.A.2
Thind, B.S.3
Forgie, A.H.4
Stirrups, D.R.5
-
2
-
-
0036528341
-
The role of MSX1 in human tooth agenesis
-
Lidral A.C., and Reising B.C. The role of MSX1 in human tooth agenesis. J Dent Res 81 (2002) 274-278
-
(2002)
J Dent Res
, vol.81
, pp. 274-278
-
-
Lidral, A.C.1
Reising, B.C.2
-
3
-
-
0037362993
-
Oral clefts and syndromic forms of tooth agenesis as models for genetics of isolated tooth agenesis
-
Vieira A.R. Oral clefts and syndromic forms of tooth agenesis as models for genetics of isolated tooth agenesis. J Dent Res 82 (2003) 162-165
-
(2003)
J Dent Res
, vol.82
, pp. 162-165
-
-
Vieira, A.R.1
-
5
-
-
35348870990
-
Defining subphenotypes for oral clefts based on dental development
-
Letra A., Menezes R., Granjeiro J.M., and Vieira A.R. Defining subphenotypes for oral clefts based on dental development. J Dent Res 86 (2007) 986-991
-
(2007)
J Dent Res
, vol.86
, pp. 986-991
-
-
Letra, A.1
Menezes, R.2
Granjeiro, J.M.3
Vieira, A.R.4
-
6
-
-
0034445306
-
Clinical, radiographic, and genetic evaluation of a novel form of autosomal-dominant oligodontia
-
Goldenberg M., Das P., Messersmith M., Stockton D.W., Patel P.I., and D'Souza R.N. Clinical, radiographic, and genetic evaluation of a novel form of autosomal-dominant oligodontia. J Dent Res 79 (2000) 1469-1475
-
(2000)
J Dent Res
, vol.79
, pp. 1469-1475
-
-
Goldenberg, M.1
Das, P.2
Messersmith, M.3
Stockton, D.W.4
Patel, P.I.5
D'Souza, R.N.6
-
7
-
-
0024835459
-
A controlled study of the association of various dental anomalies with hypodontia of permanent teeth
-
Lai P.Y., and Seow W.K. A controlled study of the association of various dental anomalies with hypodontia of permanent teeth. Pediatr Dent 11 (1989) 291-296
-
(1989)
Pediatr Dent
, vol.11
, pp. 291-296
-
-
Lai, P.Y.1
Seow, W.K.2
-
8
-
-
0034951583
-
Characteristics of incisor-premolar hypodontia in families
-
Arte S., Nieminen P., Apajalahti S., Haavikko K., Thesleff I., and Pirinen S. Characteristics of incisor-premolar hypodontia in families. J Dent Res 80 (2001) 1445-1450
-
(2001)
J Dent Res
, vol.80
, pp. 1445-1450
-
-
Arte, S.1
Nieminen, P.2
Apajalahti, S.3
Haavikko, K.4
Thesleff, I.5
Pirinen, S.6
-
9
-
-
0035222443
-
Variations in number and morphology of permanent teeth in 7-year-old Swedish children
-
Backman B., and Wahlin Y.B. Variations in number and morphology of permanent teeth in 7-year-old Swedish children. Int J Paediatr Dent 11 (2001) 11-17
-
(2001)
Int J Paediatr Dent
, vol.11
, pp. 11-17
-
-
Backman, B.1
Wahlin, Y.B.2
-
10
-
-
0024724860
-
Association of taurodontism with hypodontia: a controlled study
-
Seow W.K., and Lai P.Y. Association of taurodontism with hypodontia: a controlled study. Pediatr Dent 11 (1989) 214-219
-
(1989)
Pediatr Dent
, vol.11
, pp. 214-219
-
-
Seow, W.K.1
Lai, P.Y.2
-
11
-
-
0027636307
-
Taurodontism and length of teeth in patients with oligodontia
-
Schalk-van der Weide Y., Steen W.H., and Bosman F. Taurodontism and length of teeth in patients with oligodontia. J Oral Rehabil 20 (1993) 401-412
-
(1993)
J Oral Rehabil
, vol.20
, pp. 401-412
-
-
Schalk-van der Weide, Y.1
Steen, W.H.2
Bosman, F.3
-
12
-
-
0036884421
-
Concomitant occurrence of canine malposition and tooth agenesis: evidence of orofacial genetic fields
-
Peck S., Peck L., and Kataja M. Concomitant occurrence of canine malposition and tooth agenesis: evidence of orofacial genetic fields. Am J Orthod Dentofacial Orthop 122 (2002) 657-660
-
(2002)
Am J Orthod Dentofacial Orthop
, vol.122
, pp. 657-660
-
-
Peck, S.1
Peck, L.2
Kataja, M.3
-
13
-
-
33645463472
-
Dental transposition as a disorder of genetic origin
-
Ely N.J., Sherriff M., and Cobourne M.T. Dental transposition as a disorder of genetic origin. Eur J Orthod 28 (2006) 145-151
-
(2006)
Eur J Orthod
, vol.28
, pp. 145-151
-
-
Ely, N.J.1
Sherriff, M.2
Cobourne, M.T.3
-
14
-
-
0022749047
-
A retrospective study of double teeth in the primary dentition
-
Razak I.A., and Nik-Hussein N.N. A retrospective study of double teeth in the primary dentition. Ann Acad Med Singapore 15 (1986) 393-396
-
(1986)
Ann Acad Med Singapore
, vol.15
, pp. 393-396
-
-
Razak, I.A.1
Nik-Hussein, N.N.2
-
15
-
-
34047127502
-
Prevalence and distribution of dental anomalies in orthodontic patients
-
Altug-Atac A.T., and Erdem D. Prevalence and distribution of dental anomalies in orthodontic patients. Am J Orthod Dentofacial Orthop 131 (2007) 510-514
-
(2007)
Am J Orthod Dentofacial Orthop
, vol.131
, pp. 510-514
-
-
Altug-Atac, A.T.1
Erdem, D.2
-
16
-
-
0030098105
-
Survey of anomalies in primary teeth and their correlation with the permanent dentition
-
Whittington B.R., and Durward C.S. Survey of anomalies in primary teeth and their correlation with the permanent dentition. N Z Dent J 92 (1996) 4-8
-
(1996)
N Z Dent J
, vol.92
, pp. 4-8
-
-
Whittington, B.R.1
Durward, C.S.2
-
17
-
-
0029083386
-
Gene defect in hypodontia: exclusion of MSX1 and MSX2 as candidate genes
-
Nieminen P., Arte S., Pirinen S., Peltonen L., and Thesleff I. Gene defect in hypodontia: exclusion of MSX1 and MSX2 as candidate genes. Hum Genet 96 (1995) 305-308
-
(1995)
Hum Genet
, vol.96
, pp. 305-308
-
-
Nieminen, P.1
Arte, S.2
Pirinen, S.3
Peltonen, L.4
Thesleff, I.5
-
18
-
-
0034199841
-
The genetics of human tooth agenesis: new discoveries for understanding dental anomalies
-
Vastardis H. The genetics of human tooth agenesis: new discoveries for understanding dental anomalies. Am J Orthod Dentofacial Orthop 117 (2000) 650-656
-
(2000)
Am J Orthod Dentofacial Orthop
, vol.117
, pp. 650-656
-
-
Vastardis, H.1
-
19
-
-
33847368959
-
Interferon regulatory factor 6 (IRF6) and fibroblast growth factor receptor 1 (FGFR1) contribute to human tooth agenesis
-
Vieira A.R., Modesto A., Meira R., Barbosa A.R., Lidral A.C., and Murray J.C. Interferon regulatory factor 6 (IRF6) and fibroblast growth factor receptor 1 (FGFR1) contribute to human tooth agenesis. Am J Med Genet A 143 (2007) 538-545
-
(2007)
Am J Med Genet A
, vol.143
, pp. 538-545
-
-
Vieira, A.R.1
Modesto, A.2
Meira, R.3
Barbosa, A.R.4
Lidral, A.C.5
Murray, J.C.6
-
20
-
-
4644312296
-
MSX1, PAX9, and TGFA contribute to tooth agenesis in humans
-
Vieira A.R., Meira R., Modesto A., and Murray J.C. MSX1, PAX9, and TGFA contribute to tooth agenesis in humans. J Dent Res 83 (2004) 723-727
-
(2004)
J Dent Res
, vol.83
, pp. 723-727
-
-
Vieira, A.R.1
Meira, R.2
Modesto, A.3
Murray, J.C.4
-
21
-
-
49149124193
-
-
Instituto Brasileiro de Geografia e Estatística. Contagem da população; 2007.
-
Instituto Brasileiro de Geografia e Estatística. Contagem da população; 2007.
-
-
-
-
22
-
-
41649093368
-
Assessing the proposed association between tooth agenesis and taurodontism in 975 paediatric subjects
-
Küchler E.C., Risso P.A., Costa M.C., Modesto A., and Vieira A.R. Assessing the proposed association between tooth agenesis and taurodontism in 975 paediatric subjects. Int J Paediatr Dent 18 (2008) 231-234
-
(2008)
Int J Paediatr Dent
, vol.18
, pp. 231-234
-
-
Küchler, E.C.1
Risso, P.A.2
Costa, M.C.3
Modesto, A.4
Vieira, A.R.5
-
24
-
-
0018987530
-
Clinical significance of taurodontism
-
Durr D.P., Campos C.A., and Ayers C.S. Clinical significance of taurodontism. J Am Dent Assoc 100 March (1980) 378-381
-
(1980)
J Am Dent Assoc
, vol.100
, Issue.March
, pp. 378-381
-
-
Durr, D.P.1
Campos, C.A.2
Ayers, C.S.3
-
26
-
-
0038282835
-
The interdisciplinary management of hypodontia: background and role of paediatric dentistry
-
Nunn J.H., Carter N.E., Gillgrass T.J., Hobson R.S., Jepson N.J., Meechan J.G., et al. The interdisciplinary management of hypodontia: background and role of paediatric dentistry. Br Dent J 194 (2003) 245-251
-
(2003)
Br Dent J
, vol.194
, pp. 245-251
-
-
Nunn, J.H.1
Carter, N.E.2
Gillgrass, T.J.3
Hobson, R.S.4
Jepson, N.J.5
Meechan, J.G.6
-
27
-
-
0017932632
-
Congenital absence of teeth: a review with emphasis on inheritance patterns
-
Graber L.W. Congenital absence of teeth: a review with emphasis on inheritance patterns. J Am Dent Assoc 96 (1978) 266-275
-
(1978)
J Am Dent Assoc
, vol.96
, pp. 266-275
-
-
Graber, L.W.1
-
28
-
-
0027865406
-
Anomalies associated with hypodontia of the permanent lateral incisor and second premolar
-
Symons A.L., Stritzel F., and Stamation J. Anomalies associated with hypodontia of the permanent lateral incisor and second premolar. J Clin Pediatr Dent 17 (1993) 109-111
-
(1993)
J Clin Pediatr Dent
, vol.17
, pp. 109-111
-
-
Symons, A.L.1
Stritzel, F.2
Stamation, J.3
-
29
-
-
0025572715
-
Agenesis of the second premolar in males and females: distribution, number and sites affected
-
Stritzel F., Symons A.L., and Gage J.P. Agenesis of the second premolar in males and females: distribution, number and sites affected. J Clin Pediatr Dent 15 (1990) 39-41
-
(1990)
J Clin Pediatr Dent
, vol.15
, pp. 39-41
-
-
Stritzel, F.1
Symons, A.L.2
Gage, J.P.3
-
30
-
-
0036551103
-
Hypodontia: etiology, clinical features, and management
-
Dhanrajani P.J. Hypodontia: etiology, clinical features, and management. Quintessence Int 33 (2002) 294-302
-
(2002)
Quintessence Int
, vol.33
, pp. 294-302
-
-
Dhanrajani, P.J.1
-
31
-
-
28444440212
-
Clinical features of hypodontia and associated dental anomalies: a retrospective study
-
Kirzioglu Z., Koseler Sentut T., Ozay Erturk M.S., and Karayilmaz H. Clinical features of hypodontia and associated dental anomalies: a retrospective study. Oral Dis 11 (2005) 399-404
-
(2005)
Oral Dis
, vol.11
, pp. 399-404
-
-
Kirzioglu, Z.1
Koseler Sentut, T.2
Ozay Erturk, M.S.3
Karayilmaz, H.4
-
32
-
-
2942653509
-
Orofacial cleft in Southern Italy
-
Carinci F., Rullo R., Laino G., Festa V., Mazzarella N., Morano D., et al. Orofacial cleft in Southern Italy. Minerva Stomatol 52 (2003) 427-431
-
(2003)
Minerva Stomatol
, vol.52
, pp. 427-431
-
-
Carinci, F.1
Rullo, R.2
Laino, G.3
Festa, V.4
Mazzarella, N.5
Morano, D.6
-
33
-
-
0021159526
-
A unifying aetiological explanation for anomalies of human tooth number and size
-
Brook A.H. A unifying aetiological explanation for anomalies of human tooth number and size. Arch Oral Biol 29 (1984) 373-378
-
(1984)
Arch Oral Biol
, vol.29
, pp. 373-378
-
-
Brook, A.H.1
-
35
-
-
0027619197
-
Maxillary canine-first premolar transposition, associated dental anomalies and genetic basis
-
Peck L., Peck S., and Attia Y. Maxillary canine-first premolar transposition, associated dental anomalies and genetic basis. Angle Orthod 63 (1993) 99-109
-
(1993)
Angle Orthod
, vol.63
, pp. 99-109
-
-
Peck, L.1
Peck, S.2
Attia, Y.3
-
36
-
-
0028251886
-
The palatally displaced canine as a dental anomaly of genetic origin
-
Peck S., Peck L., and Kataja M. The palatally displaced canine as a dental anomaly of genetic origin. Angle Orthod 64 (1994) 249-256
-
(1994)
Angle Orthod
, vol.64
, pp. 249-256
-
-
Peck, S.1
Peck, L.2
Kataja, M.3
-
37
-
-
0032084268
-
Clinical management of impacted maxillary canines
-
Bishara S.E. Clinical management of impacted maxillary canines. Semin Orthod 4 (1998) 87-98
-
(1998)
Semin Orthod
, vol.4
, pp. 87-98
-
-
Bishara, S.E.1
-
38
-
-
0036053716
-
Maxillary canine transpositions in two brothers and one sister: associated dental anomalies and genetic basis
-
54-8, 12
-
Segura J.J., Hattab F., and Rios V. Maxillary canine transpositions in two brothers and one sister: associated dental anomalies and genetic basis. ASDC J Dent Child 69 (2002) 54-8, 12
-
(2002)
ASDC J Dent Child
, vol.69
-
-
Segura, J.J.1
Hattab, F.2
Rios, V.3
-
39
-
-
0014633892
-
The inheritance pattern of missing, peg-shaped and strongly mesio-distally reduced upper lateral incisors
-
Alvesalo L., and Portin P. The inheritance pattern of missing, peg-shaped and strongly mesio-distally reduced upper lateral incisors. Acta Odontol Scand 27 (1969) 563-575
-
(1969)
Acta Odontol Scand
, vol.27
, pp. 563-575
-
-
Alvesalo, L.1
Portin, P.2
-
40
-
-
0030062664
-
On the genetics of hypodontia and microdontia: synergism or allelism of major genes in a family with six affected members
-
Lyngstadaas S.P., Nordbo H., Gedde-Dahl Jr. T., and Thrane P.S. On the genetics of hypodontia and microdontia: synergism or allelism of major genes in a family with six affected members. J Med Genet 33 (1996) 137-142
-
(1996)
J Med Genet
, vol.33
, pp. 137-142
-
-
Lyngstadaas, S.P.1
Nordbo, H.2
Gedde-Dahl Jr., T.3
Thrane, P.S.4
-
41
-
-
33746780211
-
Ectopia or concomitant hypohyperdontia? A case report
-
Bateman G., and Mossey P.A. Ectopia or concomitant hypohyperdontia? A case report. J Orthod 33 (2006) 71-77
-
(2006)
J Orthod
, vol.33
, pp. 71-77
-
-
Bateman, G.1
Mossey, P.A.2
-
42
-
-
0024232824
-
Numeric anomalies of teeth in concomitant hypodontia and hyperdontia
-
Ranta R. Numeric anomalies of teeth in concomitant hypodontia and hyperdontia. J Craniofac Genet Dev Biol 8 (1988) 245-251
-
(1988)
J Craniofac Genet Dev Biol
, vol.8
, pp. 245-251
-
-
Ranta, R.1
|