Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Inheritance pattern and elemental composition of enamel affected by hypomaturation amelogenesis imperfecta.

Connective tissue research - 1 Jan 2002

Shore R C, Bäckman B, Brookes S J, Kirkham J, Wood S R, Robinson C

Abstract excerpt

Hypomaturation amelogenesis imperfecta (AI) is characterized clinically by enamel of normal thickness that is hypomineralized, mottled, and detaches easily from the underlying dentin. Autosomal dominant, autosomal recessive, X-linked, and sporadic modes of inheritance have been documented. The present study investigated the elemental composition of the enamel of teeth from individuals demonstrating clinical...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Amelogenesis Imperfecta
Share to Carbon
Share to Dental Enamel

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Microscopy, Electron, Scanning

Share to Nitrogen

Share to Phenotype

Share to Radiography

Share to Reference Values

Source

Identifiers

PMID: 12489199
DOI: 10.1080/03008200290000871

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Inheritance pattern and elemental composition of enamel affected by hypomaturation amelogenesis imperfecta.PMID 12489199Read ↗

The mineral and protein content of enamel in amelogenesis imperfecta.Semantic proximity Read ↗

Molecular-based phenotype variations in amelogenesis imperfecta.Semantic proximity Read ↗

Phenotypic diversity and revision of the nomenclature for autosomal recessive amelogenesis imperfecta.Semantic proximity Read ↗

Enamel Phenotypes: Genetic and Environmental Determinants.Semantic proximity Read ↗

The structure and composition of deciduous enamel affected by local hypoplastic autosomal dominant amelogenesis imperfecta resulting from an ENAM mutation.Semantic proximity Read ↗

The molecular basis of hereditary enamel defects in humans.Semantic proximity Read ↗

Ultrastructural analysis of the teeth affected by amelogenesis imperfecta resulting from FAM83H mutations and review of the literature.Semantic proximity Read ↗

Phenotype and enamel ultrastructure characteristics in patients with ENAM gene mutations g.13185-13186insAG and 8344delG.Semantic proximity Read ↗

Hypomaturation Amelogenesis Imperfecta due to <i>WDR72</i> Mutations: A Novel Mutation and Ultrastructural Analyses of Deciduous TeethSemantic proximity Read ↗

Identification of the enamelin (g.8344delG) mutation in a new kindred and presentation of a standardized ENAM nomenclature.Semantic proximity Read ↗

Ultrastructural Analyses of Deciduous Teeth Affected by Hypocalcified Amelogenesis Imperfecta from a Family with a Novel Y458X FAM83H Nonsense MutationSemantic proximity Read ↗

Amelogenesis imperfecta.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.