158 related articles for article (PubMed ID: 10466415)
1. 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
Clin Genet; 1999 Jul; 56(1):35-40. PubMed ID: 10466415
[TBL] [Abstract][Full Text] [Related]
2. Identification of a mutation in DLX3 associated with tricho-dento-osseous (TDO) syndrome.
Price JA; Bowden DW; Wright JT; Pettenati MJ; Hart TC
Hum Mol Genet; 1998 Mar; 7(3):563-9. PubMed ID: 9467018
[TBL] [Abstract][Full Text] [Related]
3. DLX3 mutation associated with autosomal dominant amelogenesis imperfecta with taurodontism.
Dong J; Amor D; Aldred MJ; Gu T; Escamilla M; MacDougall M
Am J Med Genet A; 2005 Mar; 133A(2):138-41. PubMed ID: 15666299
[TBL] [Abstract][Full Text] [Related]
4. DLX3 mutation in a new family and its phenotypic variations.
Lee SK; Lee ZH; Lee SJ; Ahn BD; Kim YJ; Lee SH; Kim JW
J Dent Res; 2008 Apr; 87(4):354-7. PubMed ID: 18362318
[TBL] [Abstract][Full Text] [Related]
5. Severely hypoplastic amelogenesis imperfecta with taurodontism.
Pavlic A; Lukinmaa PL; Nieminen P; Kiukkonen A; Alaluusua S
Int J Paediatr Dent; 2007 Jul; 17(4):259-66. PubMed ID: 17559453
[TBL] [Abstract][Full Text] [Related]
6. Novel DLX3 variants in amelogenesis imperfecta with attenuated tricho-dento-osseous syndrome.
Whitehouse LLE; Smith CEL; Poulter JA; Brown CJ; Patel A; Lamb T; Brown LR; O'Sullivan EA; Mitchell RE; Berry IR; Charlton R; Inglehearn CF; Mighell AJ
Oral Dis; 2019 Jan; 25(1):182-191. PubMed ID: 30095208
[TBL] [Abstract][Full Text] [Related]
7. DLX3 c.561_562delCT mutation causes attenuated phenotype of tricho-dento-osseous syndrome.
Wright JT; Hong SP; Simmons D; Daly B; Uebelhart D; Luder HU
Am J Med Genet A; 2008 Feb; 146A(3):343-9. PubMed ID: 18203197
[TBL] [Abstract][Full Text] [Related]
8. A common DLX3 gene mutation is responsible for tricho-dento-osseous syndrome in Virginia and North Carolina families.
Price JA; Wright JT; Kula K; Bowden DW; Hart TC
J Med Genet; 1998 Oct; 35(10):825-8. PubMed ID: 9783705
[TBL] [Abstract][Full Text] [Related]
9. Analysis of the tricho-dento-osseous syndrome genotype and phenotype.
Wright JT; Kula K; Hall K; Simmons JH; Hart TC
Am J Med Genet; 1997 Oct; 72(2):197-204. PubMed ID: 9382143
[TBL] [Abstract][Full Text] [Related]
10. Morphological analyses and a novel de novo DLX3 mutation associated with tricho-dento-osseous syndrome in a Chinese family.
Li Y; Han D; Zhang H; Liu H; Wong S; Zhao N; Qiu L; Feng H
Eur J Oral Sci; 2015 Aug; 123(4):228-34. PubMed ID: 26104267
[TBL] [Abstract][Full Text] [Related]
11. Taurodontism of the mandibular first permanent molar distinguishes between the tricho-dento-osseous (TDO) syndrome and amelogenesis imperfecta.
Seow WK
Clin Genet; 1993 May; 43(5):240-6. PubMed ID: 8375104
[TBL] [Abstract][Full Text] [Related]
12. Craniofacial variations in the tricho-dento-osseous syndrome.
Nguyen T; Phillips C; Frazier-Bower S; Wright T
Clin Genet; 2013 Apr; 83(4):375-9. PubMed ID: 22671030
[TBL] [Abstract][Full Text] [Related]
13. Increased bone density associated with DLX3 mutation in the tricho-dento-osseous syndrome.
Haldeman RJ; Cooper LF; Hart TC; Phillips C; Boyd C; Lester GE; Wright JT
Bone; 2004 Oct; 35(4):988-97. PubMed ID: 15454107
[TBL] [Abstract][Full Text] [Related]
14. DLX3 homeodomain mutations cause tricho-dento-osseous syndrome with novel phenotypes.
Nieminen P; Lukinmaa PL; Alapulli H; Methuen M; Suojärvi T; Kivirikko S; Peltola J; Asikainen M; Alaluusua S
Cells Tissues Organs; 2011; 194(1):49-59. PubMed ID: 21252474
[TBL] [Abstract][Full Text] [Related]
15. Genetic linkage of the tricho-dento-osseous syndrome to chromosome 17q21.
Hart TC; Bowden DW; Bolyard J; Kula K; Hall K; Wright JT
Hum Mol Genet; 1997 Dec; 6(13):2279-84. PubMed ID: 9361034
[TBL] [Abstract][Full Text] [Related]
16. Unexpected identification of a recurrent mutation in the DLX3 gene causing amelogenesis imperfecta.
Kim YJ; Seymen F; Koruyucu M; Kasimoglu Y; Gencay K; Shin TJ; Hyun HK; Lee ZH; Kim JW
Oral Dis; 2016 May; 22(4):297-302. PubMed ID: 26762616
[TBL] [Abstract][Full Text] [Related]
17. Transcriptional factor DLX3 promotes the gene expression of enamel matrix proteins during amelogenesis.
Zhang Z; Tian H; Lv P; Wang W; Jia Z; Wang S; Zhou C; Gao X
PLoS One; 2015; 10(3):e0121288. PubMed ID: 25815730
[TBL] [Abstract][Full Text] [Related]
18. Amelogenesis imperfecta with taurodontism and the tricho-dento-osseous syndrome: separate conditions or a spectrum of disease?
Crawford PJ; Aldred MJ
Clin Genet; 1990 Jul; 38(1):44-50. PubMed ID: 2387085
[TBL] [Abstract][Full Text] [Related]
19. Novel DLX3 variant identified in a family with tricho-dento-osseous syndrome.
Liu H; Wang Y; Liu H; Yu M; Zheng J; Feng H; Liu Y; Han D
Arch Oral Biol; 2022 Sep; 141():105479. PubMed ID: 35714441
[TBL] [Abstract][Full Text] [Related]
20. Clinical features of tricho-dento-osseous syndrome and presentation of three new cases: an addition to clinical heterogeneity.
Islam M; Lurie AG; Reichenberger E
Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 2005 Dec; 100(6):736-42. PubMed ID: 16301156
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]