PubMed

Hereditary dentine disorders: dentinogenesis imperfecta and dentine dysplasia.

Barron MJ, McDonnell ST, Mackie I, Dixon MJ.

Orphanet J Rare Dis. 2008 Nov 20;3:31. Review.PMID: 19021896 [PubMed - indexed for MEDLINE]Related articlesFree article

Hereditary dentin defects.

Kim JW, Simmer JP.

J Dent Res. 2007 May;86(5):392-9. Review.PMID: 17452557 [PubMed - indexed for MEDLINE]Related articles

Phenotypic variation in dentinogenesis imperfecta/dentin dysplasia linked to 4q21.

Beattie ML, Kim JW, Gong SG, Murdoch-Kinch CA, Simmer JP, Hu JC.

J Dent Res. 2006 Apr;85(4):329-33.PMID: 16567553 [PubMed - indexed for MEDLINE]Related articlesFree article

Disorders of human dentin.

Hart PS, Hart TC.

Cells Tissues Organs. 2007;186(1):70-7.PMID: 17627120 [PubMed - indexed for MEDLINE]Related articles

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. Epub 2004 Dec 8.PMID: 15592686 [PubMed - indexed for MEDLINE]Related articles

Overlapping DSPP mutations cause dentin dysplasia and dentinogenesis imperfecta.

McKnight DA, Simmer JP, Hart PS, Hart TC, Fisher LW.

J Dent Res. 2008 Dec;87(12):1108-11. Erratum in: J Dent Res. 2009 Jan;88(1):95. PMID: 19029076 [PubMed - indexed for MEDLINE]Related articlesFree article

Splicing site mutations in dentin sialophosphoprotein causing dentinogenesis imperfecta type II.

Holappa H, Nieminen P, Tolva L, Lukinmaa PL, Alaluusua S.

Eur J Oral Sci. 2006 Oct;114(5):381-4.PMID: 17026502 [PubMed - indexed for MEDLINE]Related articles

Dental structural diseases mapping to human chromosome 4q21.

MacDougall M.

Connect Tissue Res. 2003;44 Suppl 1:285-91. Review.PMID: 12952210 [PubMed - indexed for MEDLINE]Related articles

Refined mapping of the human dentin sialophosphoprotein (DSPP) gene within the critical dentinogenesis imperfecta type II and dentin dysplasia type II loci.

MacDougall M.

Eur J Oral Sci. 1998 Jan;106 Suppl 1:227-33.PMID: 9541230 [PubMed - indexed for MEDLINE]Related articles

A novel splice acceptor mutation in the DSPP gene causing dentinogenesis imperfecta type II.

Kim JW, Nam SH, Jang KT, Lee SH, Kim CC, Hahn SH, Hu JC, Simmer JP.

Hum Genet. 2004 Aug;115(3):248-54. Epub 2004 Jul 6.PMID: 15241678 [PubMed - indexed for MEDLINE]Related articles

A novel DSPP mutation is associated with type II dentinogenesis imperfecta in a Chinese family.

Zhang X, Chen L, Liu J, Zhao Z, Qu E, Wang X, Chang W, Xu C, Wang QK, Liu M.

BMC Med Genet. 2007 Aug 8;8:52.PMID: 17686168 [PubMed - indexed for MEDLINE]Related articlesFree article

Molecular basis of human dentin diseases.

MacDougall M, Dong J, Acevedo AC.

Am J Med Genet A. 2006 Dec 1;140(23):2536-46. Review.PMID: 16955410 [PubMed - indexed for MEDLINE]Related articles

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.PMID: 10765957 [PubMed - indexed for MEDLINE]Related articlesFree article

Heritable dentin defects: nosology, pathology, and treatment.

Ranta H, Lukinmaa PL, Waltimo J.

Am J Med Genet. 1993 Jan 15;45(2):193-200. Review.PMID: 8456802 [PubMed - indexed for MEDLINE]Related articles

The dentition in the osteogenesis imperfecta syndromes.

Levin LS.

Clin Orthop Relat Res. 1981 Sep;(159):64-74.PMID: 7285471 [PubMed - indexed for MEDLINE]Related articles

Dentin phosphoprotein compound mutation in dentin sialophosphoprotein causes dentinogenesis imperfecta type III.

Dong J, Gu T, Jeffords L, MacDougall M.

Am J Med Genet A. 2005 Jan 30;132A(3):305-9.PMID: 15690376 [PubMed - indexed for MEDLINE]Related articles

Opalescent dentine in two affected siblings.

Mahoney EK, Widmer RP, Sillence DO.

N Z Dent J. 2001 Mar;97(427):15-8.PMID: 11355244 [PubMed - indexed for MEDLINE]Related articles

A dentin sialophosphoprotein mutation that partially disrupts a splice acceptor site causes type II dentin dysplasia.

Lee SK, Hu JC, Lee KE, Simmer JP, Kim JW.

J Endod. 2008 Dec;34(12):1470-3. Epub 2008 Sep 26.PMID: 19026876 [PubMed - indexed for MEDLINE]Related articlesFree article

Dentin dysplasia, type II linkage to chromosome 4q.

Dean JA, Hartsfield JK Jr, Wright JT, Hart TC.

J Craniofac Genet Dev Biol. 1997 Oct-Dec;17(4):172-7.PMID: 9493074 [PubMed - indexed for MEDLINE]Related articles

Novel COL1A1 mutation (G559C) [correction of G599C] associated with mild osteogenesis imperfecta and dentinogenesis imperfecta.

Pallos D, Hart PS, Cortelli JR, Vian S, Wright JT, Korkko J, Brunoni D, Hart TC.

Arch Oral Biol. 2001 May;46(5):459-70.PMID: 11286811 [PubMed - indexed for MEDLINE]Related articles