Amelogenesis imperfecta: autosomal dominant hypomaturation-hypoplasia type with taurodontism.

Suppr

超能文献

作者信息

Crawford P J, Evans R D, Aldred M J

出版信息

Br Dent J. 1988 Feb 6;164(3):71-3. doi: 10.1038/sj.bdj.4806360.

DOI:10.1038/sj.bdj.4806360

PMID:3422811

Abstract

摘要

相似文献

Amelogenesis imperfecta: autosomal dominant hypomaturation-hypoplasia type with taurodontism.

Br Dent J. 1988 Feb 6;164(3):71-3. doi: 10.1038/sj.bdj.4806360.

Variable expression in Amelogenesis imperfecta with taurodontism.

J Oral Pathol. 1988 Aug;17(7):327-33. doi: 10.1111/j.1600-0714.1988.tb01545.x.

Hypoplastic-hypomaturation amelogenesis imperfecta with taurodontism: report of case.

ASDC J Dent Child. 1975 Sep-Oct;42(5):379-83.

'Amelogenesis imperfecta: autosomal dominant hypomaturation-hypoplasia type with taurodontism'.

Br Dent J. 1988 May 21;164(10):310. doi: 10.1038/sj.bdj.4806436.

Amelogenesis imperfecta with enamel opacities and taurodontism: an alternative diagnosis for 'idiopathic dental fluorosis'.

Br Dent J. 1996 Sep 7;181(5):167-72. doi: 10.1038/sj.bdj.4809200.

Amelogenesis imperfecta with taurodontism.

Oral Surg Oral Med Oral Pathol. 1979 Dec;48(6):540-4. doi: 10.1016/0030-4220(79)90301-3.

Unusual manifestations in X-linked amelogenesis imperfecta.

Int J Paediatr Dent. 2003 Sep;13(5):356-61. doi: 10.1046/j.1365-263x.2003.00484.x.

Interradicular dentin dysplasia associated with amelogenesis imperfecta with taurodontism or trichodentoosseous syndrome: a diagnostic dilemma.

Indian J Dent Res. 2014 Mar-Apr;25(2):269-71. doi: 10.4103/0970-9290.135942.

Amelogenesis imperfecta: a clinician's challenge.

J Indian Soc Pedod Prev Dent. 2012 Jan-Mar;30(1):70-3. doi: 10.4103/0970-4388.95587.

Analysis of a kindred with amelogenesis imperfecta.

J Oral Pathol. 1985 May;14(5):366-74. doi: 10.1111/j.1600-0714.1985.tb00507.x.

引用本文的文献

Amelogenesis imperfecta: Report of a case and review of literature.

J Oral Maxillofac Pathol. 2009 Jul;13(2):70-7. doi: 10.4103/0973-029X.57673.

Amelogenesis imperfecta: genotype-phenotype studies in 71 families.

Cells Tissues Organs. 2011;194(2-4):279-83. doi: 10.1159/000324339. Epub 2011 May 19.

Clinical and radiographic dental findings in X linked hypohidrotic ectodermal dysplasia.

J Med Genet. 1991 Mar;28(3):181-5. doi: 10.1136/jmg.28.3.181.

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型，支持多种主流文档格式。

立即体验

相似文献

Amelogenesis imperfecta: autosomal dominant hypomaturation-hypoplasia type with taurodontism.

Br Dent J. 1988 Feb 6;164(3):71-3. doi: 10.1038/sj.bdj.4806360.

Variable expression in Amelogenesis imperfecta with taurodontism.

J Oral Pathol. 1988 Aug;17(7):327-33. doi: 10.1111/j.1600-0714.1988.tb01545.x.

Hypoplastic-hypomaturation amelogenesis imperfecta with taurodontism: report of case.

ASDC J Dent Child. 1975 Sep-Oct;42(5):379-83.

'Amelogenesis imperfecta: autosomal dominant hypomaturation-hypoplasia type with taurodontism'.

Br Dent J. 1988 May 21;164(10):310. doi: 10.1038/sj.bdj.4806436.

Amelogenesis imperfecta with enamel opacities and taurodontism: an alternative diagnosis for 'idiopathic dental fluorosis'.

Br Dent J. 1996 Sep 7;181(5):167-72. doi: 10.1038/sj.bdj.4809200.

Amelogenesis imperfecta with taurodontism.

Oral Surg Oral Med Oral Pathol. 1979 Dec;48(6):540-4. doi: 10.1016/0030-4220(79)90301-3.

Unusual manifestations in X-linked amelogenesis imperfecta.

Int J Paediatr Dent. 2003 Sep;13(5):356-61. doi: 10.1046/j.1365-263x.2003.00484.x.

Interradicular dentin dysplasia associated with amelogenesis imperfecta with taurodontism or trichodentoosseous syndrome: a diagnostic dilemma.

Indian J Dent Res. 2014 Mar-Apr;25(2):269-71. doi: 10.4103/0970-9290.135942.

Amelogenesis imperfecta: a clinician's challenge.

J Indian Soc Pedod Prev Dent. 2012 Jan-Mar;30(1):70-3. doi: 10.4103/0970-4388.95587.

Analysis of a kindred with amelogenesis imperfecta.

J Oral Pathol. 1985 May;14(5):366-74. doi: 10.1111/j.1600-0714.1985.tb00507.x.

引用本文的文献

Amelogenesis imperfecta: Report of a case and review of literature.

J Oral Maxillofac Pathol. 2009 Jul;13(2):70-7. doi: 10.4103/0973-029X.57673.

Amelogenesis imperfecta: genotype-phenotype studies in 71 families.

Cells Tissues Organs. 2011;194(2-4):279-83. doi: 10.1159/000324339. Epub 2011 May 19.

Clinical and radiographic dental findings in X linked hypohidrotic ectodermal dysplasia.

J Med Genet. 1991 Mar;28(3):181-5. doi: 10.1136/jmg.28.3.181.