137 related articles for article (PubMed ID: 17928732)
1. Dentinogenesis imperfecta type II: an affected family saga.
Kamboj M; Chandra A
J Oral Sci; 2007 Sep; 49(3):241-4. PubMed ID: 17928732
[TBL] [Abstract][Full Text] [Related]
2. Dentinogenesis Imperfecta : A Family which was Affected for Over Three Generations.
Surendra P; Shah R; N M R; Reddy VV
J Clin Diagn Res; 2013 Aug; 7(8):1808-11. PubMed ID: 24086922
[TBL] [Abstract][Full Text] [Related]
3. Hereditary opalescent dentin: a report of two cases.
Gupta S; Bhowate RR; Bhati A
J Contemp Dent Pract; 2010 Jul; 11(4):E049-55. PubMed ID: 20953564
[TBL] [Abstract][Full Text] [Related]
4. An unusual presentation of opalescent dentin and Brandywine isolate hereditary opalescent dentin in an Ashkenazic Jewish family.
Heimler A; Sciubba J; Lieber E; Kamen S
Oral Surg Oral Med Oral Pathol; 1985 Jun; 59(6):608-15. PubMed ID: 3859821
[TBL] [Abstract][Full Text] [Related]
5. Diagnostic features and pedodontic-orthodontic management in dentinogenesis imperfecta type II: a case report.
Huth KCh; Paschos E; Sagner T; Hickel R
Int J Paediatr Dent; 2002 Sep; 12(5):316-21. PubMed ID: 12199890
[TBL] [Abstract][Full Text] [Related]
6. [Hereditary opalescent dentin (dentinogenesis imperfecta type II). Anatomo-clinical study].
Kerébel B; Le Cabellec MT; Kerébel LM; Villette A
Actual Odontostomatol (Paris); 1978; (124):539-58. PubMed ID: 751484
[No Abstract] [Full Text] [Related]
7. Dentinogenesis imperfecta: a review and case report of a family over four generations.
Bhandari S; Pannu K
Indian J Dent Res; 2008; 19(4):357-61. PubMed ID: 19075443
[TBL] [Abstract][Full Text] [Related]
8. Mutational hot spot in the DSPP gene causing dentinogenesis imperfecta type II.
Kim JW; Hu JC; Lee JI; Moon SK; Kim YJ; Jang KT; Lee SH; Kim CC; Hahn SH; Simmer JP
Hum Genet; 2005 Feb; 116(3):186-91. PubMed ID: 15592686
[TBL] [Abstract][Full Text] [Related]
9. Dentin dysplasia, type II linkage to chromosome 4q.
Dean JA; Hartsfield JK; Wright JT; Hart TC
J Craniofac Genet Dev Biol; 1997; 17(4):172-7. PubMed ID: 9493074
[TBL] [Abstract][Full Text] [Related]
10. The non-collagenous dentin matrix proteins are involved in dentinogenesis imperfecta type II (DGI-II).
Thotakura SR; Mah T; Srinivasan R; Takagi Y; Veis A; George A
J Dent Res; 2000 Mar; 79(3):835-9. PubMed ID: 10765957
[TBL] [Abstract][Full Text] [Related]
11. Six generations of hereditary opalescent dentin: report of case.
Giansanti JS; Budnick SD
J Am Dent Assoc; 1975 Feb; 90(2):439-42. PubMed ID: 1053785
[No Abstract] [Full Text] [Related]
12. Opalescent dentine in two affected siblings.
Mahoney EK; Widmer RP; Sillence DO
N Z Dent J; 2001 Mar; 97(427):15-8. PubMed ID: 11355244
[TBL] [Abstract][Full Text] [Related]
13. A novel mutation in the DSPP gene associated with dentinogenesis imperfecta type II.
Lee SK; Lee KE; Jeon D; Lee G; Lee H; Shin CU; Jung YJ; Lee SH; Hahn SH; Kim JW
J Dent Res; 2009 Jan; 88(1):51-5. PubMed ID: 19131317
[TBL] [Abstract][Full Text] [Related]
14. Esthetic reconstruction of teeth in patient with dentinogenesis imperfecta--a case report.
Knezević A; Tarle Z; Pandurić V
Coll Antropol; 2006 Mar; 30(1):231-4. PubMed ID: 16617603
[TBL] [Abstract][Full Text] [Related]
15. A histological continuum between dentinogenesis imperfecta and dentin dysplasia: A case report with literature review.
Gulati N; Juneja S; Singh A; Singh I
Indian J Dent Res; 2019; 30(4):643-646. PubMed ID: 31745067
[TBL] [Abstract][Full Text] [Related]
16. [Hereditary pathology of the enamel and dentin. A review of molecular genetic research].
Beliakov IuA; Elizarova VM; Krotov VA; Blinnikova OE
Stomatologiia (Mosk); 2000; 79(1):8-9. PubMed ID: 10693338
[TBL] [Abstract][Full Text] [Related]
17. Radiological features of hereditary opalescent dentin.
Tanaka T; Murakami T
Dentomaxillofac Radiol; 1998 Jul; 27(4):251-3. PubMed ID: 9780905
[TBL] [Abstract][Full Text] [Related]
18. De novo mutation in the DSPP gene associated with dentinogenesis imperfecta type II in a Japanese family.
Kida M; Tsutsumi T; Shindoh M; Ikeda H; Ariga T
Eur J Oral Sci; 2009 Dec; 117(6):691-4. PubMed ID: 20121932
[TBL] [Abstract][Full Text] [Related]
19. Refinement of the dentinogenesis imperfecta type II locus to an interval of less than 2 centiMorgans at chromosome 4q21 and the creation of a yeast artificial chromosome contig of the critical region.
Aplin HM; Hirst KL; Dixon MJ
J Dent Res; 1999 Jun; 78(6):1270-6. PubMed ID: 10371252
[TBL] [Abstract][Full Text] [Related]
20. Dentinogenesis imperfecta type II- genotype and phenotype analyses in three Danish families.
Taleb K; Lauridsen E; Daugaard-Jensen J; Nieminen P; Kreiborg S
Mol Genet Genomic Med; 2018 May; 6(3):339-349. PubMed ID: 29512331
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]