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Items: 11

1.

A comprehensive analysis of normal variation and disease-causing mutations in the human DSPP gene.

McKnight DA, Suzanne Hart P, Hart TC, Hartsfield JK, Wilson A, Wright JT, Fisher LW.

Hum Mutat. 2008 Dec;29(12):1392-404. doi: 10.1002/humu.20783.

PMID:
18521831
2.

Hereditary dentine diseases resulting from mutations in DSPP gene.

Maciejewska I, Chomik E.

J Dent. 2012 Jul;40(7):542-8. doi: 10.1016/j.jdent.2012.04.004. Review.

PMID:
22521702
3.

Isolated dentinogenesis imperfecta and dentin dysplasia: revision of the classification.

de La Dure-Molla M, Philippe Fournier B, Berdal A.

Eur J Hum Genet. 2015 Apr;23(4):445-51. doi: 10.1038/ejhg.2014.159. Review.

4.

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
5.

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. doi: 10.1186/1750-1172-3-31. Review.

6.

Hereditary dentin defects.

Kim JW, Simmer JP.

J Dent Res. 2007 May;86(5):392-9. Review.

PMID:
17452557
7.

Dental structural diseases mapping to human chromosome 4q21.

MacDougall M.

Connect Tissue Res. 2003;44 Suppl 1:285-91. Review.

PMID:
12952210
8.

Post-translational modifications of sibling proteins and their roles in osteogenesis and dentinogenesis.

Qin C, Baba O, Butler WT.

Crit Rev Oral Biol Med. 2004 Jun 4;15(3):126-36. Review.

PMID:
15187031
9.

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
10.

Dentin phosphoprotein in dentin development: implications in dentinogenesis imperfecta.

MacDougall M.

Proc Finn Dent Soc. 1992;88 Suppl 1:195-208. Review.

PMID:
1508875
11.

The molecular genetic basis and diagnosis of familial hypercholesterolemia in Denmark.

Jensen HK.

Dan Med Bull. 2002 Nov;49(4):318-45. Review.

PMID:
12553167

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