Literature DB >> 6362739

A new classification of heritable human enamel defects and a discussion of dentin defects.

E D Shields.   

Abstract

rude paradigms for both nonsyndromic human heritable primary enamel defects and heritable primary dentin defects have been presented. Since such classifications are merely attempts to identify biologic patterns, their accuracy only can be determined mathematically, and thus must wait for pertinent quantifiable data.

Entities:  

Mesh:

Year:  1983        PMID: 6362739

Source DB:  PubMed          Journal:  Birth Defects Orig Artic Ser        ISSN: 0547-6844


  3 in total

1.  Osteogenesis imperfecta: potential therapeutic approaches.

Authors:  Maxime Rousseau; Jean-Marc Retrouvey
Journal:  PeerJ       Date:  2018-08-17       Impact factor: 2.984

Review 2.  Dentin dysplasia type I-A dental disease with genetic heterogeneity.

Authors:  D Chen; X Li; F Lu; Y Wang; F Xiong; Q Li
Journal:  Oral Dis       Date:  2018-04-10       Impact factor: 3.511

3.  Combined treatment with laser sintering and zirconium: a case report of dentinogenesis imperfecta.

Authors:  Simel Ayyildiz; Cem Sahin; Ozlem Marti Akgün; Feridun Basak
Journal:  Case Rep Dent       Date:  2013-03-06
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.