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Analyses of oligodontia phenotypes and genetic etiologies

Analyses of oligodontia phenotypes and genetic etiologies

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_b4fae4e706cc42399f6b5e82f45aca92

Analyses of oligodontia phenotypes and genetic etiologies

About this item

Full title

Analyses of oligodontia phenotypes and genetic etiologies

Publisher

London: Nature Publishing Group UK

Journal title

International journal of oral science, 2021-09, Vol.13 (1), p.32-32, Article 32

Language

English

Formats

Publication information

Publisher

London: Nature Publishing Group UK

More information

Scope and Contents

Contents

Oligodontia is the congenital absence of six or more teeth and comprises the more severe forms of tooth agenesis. Many genes have been implicated in the etiology of tooth agenesis, which is highly variable in its clinical presentation. The purpose of this study was to identify associations between genetic mutations and clinical features of oligodon...

Alternative Titles

Full title

Analyses of oligodontia phenotypes and genetic etiologies

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_b4fae4e706cc42399f6b5e82f45aca92

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_b4fae4e706cc42399f6b5e82f45aca92

Other Identifiers

ISSN

1674-2818

E-ISSN

2049-3169

DOI

10.1038/s41368-021-00135-3

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