References
- 1
Alaluusua S.
Amoxicillin may be a cause of enamel hypomineralization.
Duodecim.
2006;
122
491-492
- 2
Alaluusua S, Lukinmaa PL.
Developmental dental toxicity of dioxin and related compounds - a review.
Int Dent J.
2006;
56
323-331
- 3
Arte S, Pirinen S.
Hypodontia. Orphanet encyclopedia 2003.
http://www.orpha.net/data/patho/GB/uk-hypodontia.pdf:update
2004;
- 4
Bartlett JD, Ganss B, Goldberg M, Moradian-Oldak J, Paine ML, Snead ML. et al .
Protein-protein interactions of the developing enamel matrix.
Curr Top Dev Biol.
2006;
74
57-115
- 5
Bloch-Zupan A, Stachtou J, Emmanouil D, Arveiler B, Griffiths D, Lacombe D.
Oro-dental features as useful diagnostic tool in Rubinstein-Taybi syndrome.
Am J Med Genet A.
2007;
143
570-573
- 6
Brancati F, Sarkozy A, Dallapiccola B.
KBG syndrome.
Orphanet J Rare Dis.
2006;
1
50
- 7
Butler WT, Brunn JC, Qin C.
Dentin extracellular matrix (ECM) proteins: comparison to bone ECM and contribution
to dynamics of dentinogenesis.
Connect Tissue Res.
2003;
44
((Suppl 1))
171-178
- 8
Cobourne MT, Mitsiadis T.
Neural crest cells and patterning of the mammalian dentition.
J Exp Zoolog B Mol Dev Evol.
2006;
306
251-260
- 9
Courtney JM, Blackburn J, Sharpe PT.
The ectodysplasin and NFkappaB signalling pathways in odontogenesis.
Arch Oral Biol.
2005;
50
159-163
- 10
Crawford PJ, Aldred MJ, Bloch-Zupan A.
Amelogenesis imperfecta.
Orphanet J Rare Dis.
2007;
- 11
Donnai D, Tomlin PI, Winter RM.
Kohlschutter syndrome in siblings.
Clin Dysmorphol.
2005;
14
123-126
- 12 Fryns JP, Ravel TJ de.
London Dysmorphology Database, London Neurogenetics Database and Dysmorphology Photo
Library on CD-ROM [Version 3] 2001. Hum Genet. R. M. Winter, M. Baraitser Oxford University Press 2002 111: 113
- 13 Gorlin RJ, Cohen MM, Hennekam JRCM. Syndromes of the head and neck 4th edn. Oxford:
University Press 2001
- 14
Haberlandt E, Svejda C, Felber S, Baumgartner S, Gunther B, Utermann G. et al .
Yellow teeth, seizures, and mental retardation: a less severe case of Kohlschutter-Tonz
syndrome.
Am J Med Genet A.
2006;
140
281-283
- 15
Hall RK.
Solitary median maxillary central incisor (SMMCI) syndrome.
Orphanet J Rare Dis.
2006;
1
12
- 16
Helfrich MH.
Osteoclast diseases and dental abnormalities.
Arch Oral Biol.
2005;
50
115-122
- 17
Hennekam RC, Robert J.
Gorlin (1923-2006): teacher, colleague, and friend.
Am J Med Genet A.
2006;
140
2514-2515
- 18
Idrees F, Bloch-Zupan A, Free SL, Vaideanu D, Thompson PJ, Ashley P. et al .
A novel homeobox mutation in the PITX2 gene in a family with Axenfeld-Rieger syndrome
associated with brain, ocular, and dental phenotypes.
Am J Med Genet B Neuropsychiatr Genet.
2006;
141
184-191
- 19
Luan X, Ito Y, Diekwisch TG.
Evolution and development of Hertwig's epithelial root sheath.
Dev Dyn.
2006;
235
1167-1180
- 20
MacDougall M, Dong J, Acevedo AC.
Molecular basis of human dentin diseases.
Am J Med Genet A.
2006;
140
2536-2546
- 21
Magloire H, Couble ML, Romeas A, Bleicher F.
Odontoblast primary cilia: facts and hypotheses.
Cell Biol Int.
2004;
28
93-99
- 22
Michaelides M, Bloch-Zupan A, Holder GE, Hunt DM, Moore AT.
An autosomal recessive cone-rod dystrophy associated with amelogenesis imperfecta.
J Med Genet.
2004;
41
468-473
- 23
Miletich I, Sharpe PT.
Normal and abnormal dental development.
Hum Mol Genet.
2003;
12
((Spec No 1))
69-73
- 24
Nieminen P, Pekkanen M, Aberg T, Thesleff I.
A graphical WWW-database on gene expression in tooth.
Eur J Oral Sci.
1998;
106
((Suppl 1))
7-11
- 25
Pispa J, Thesleff I.
Mechanisms of ectodermal organogenesis.
Dev Biol.
2003;
262
195-205
- 26
Thesleff I.
The genetic basis of tooth development and dental defects.
Am J Med Genet A.
2006;
140
2530-2535
- 27
Thesleff I, Jernvall J.
The enamel knot: a putative signaling center regulating tooth development.
Cold Spring Harb Symp Quant Biol.
1997;
62
257-267
- 28
Tucker A, Sharpe P.
The cutting-edge of mammalian development; how the embryo makes teeth.
Nat Rev Genet.
2004;
5
499-508
- 29
Wise GE.
The biology of tooth eruption.
J Dent Res.
1998;
77
1576-1579
- 30
Wolf NI, Harting I, Innes AM, Patzer S, Zeitler P, Schneider A. et al .
Ataxia, delayed dentition and hypomyelination: a novel leukoencephalopathy.
Neuropediatrics.
2007;
38
64-70
- 31
Wright JT.
The molecular etiologies and associated phenotypes of amelogenesis imperfecta.
Am J Med Genet A.
2006;
140
2547-2555
1 Re: Wolf NI, Harting I, Innes AM, Patzer S, Zeitler P, Schneider A, Wolff A, Baier
K, Zschocke J, Ebinger F, Boltshauser E, Rating D: Ataxia, Delayed Dentition and Hypomyelination:
A Novel Leukoencephalopathy
Correspondence
A. Bloch-Zupan
Faculté de Chirurgie Dentaire
Université Louis Pasteur
Centre de référence des manifestations odontologiques des maladies rares
Service de Soins Bucco-Dentaires
Centre Hospitalier Universitaire
67000 Strasbourg
France
Telefon: +33/390/24 38 87
Fax: +33/390/24 39 00
eMail: Agnes.Bloch-Zupan@dentaire-ulp.u-strasbg.fr