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Amelogenesis imperfecta

Amelogenesis imperfecta

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_d4e5dbfafc2d4129915507623dbfa9cd

Amelogenesis imperfecta

About this item

Full title

Amelogenesis imperfecta

Publisher

England: BioMed Central Ltd

Journal title

Orphanet journal of rare diseases, 2007-04, Vol.2 (1), p.17-17, Article 17

Language

English

Formats

Publication information

Publisher

England: BioMed Central Ltd

More information

Scope and Contents

Contents

Amelogenesis imperfecta (AI) represents a group of developmental conditions, genomic in origin, which affect the structure and clinical appearance of enamel of all or nearly all the teeth in a more or less equal manner, and which may be associated with morphologic or biochemical changes elsewhere in the body. The prevalence varies from 1:700 to 1:1...

Alternative Titles

Full title

Amelogenesis imperfecta

Authors, Artists and Contributors

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_d4e5dbfafc2d4129915507623dbfa9cd

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_d4e5dbfafc2d4129915507623dbfa9cd

Other Identifiers

ISSN

1750-1172

E-ISSN

1750-1172

DOI

10.1186/1750-1172-2-17

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