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

Craniofacial characteristics and genotypes of amelogenesis imperfecta patients.

European journal of orthodontics - 1 Jun 2011

Pavlic Alenka, Battelino Tadej, Trebusak Podkrajsek Katarina, Ovsenik Maja

Abstract excerpt

The aims of the study were to identify craniofacial characteristics in patients with the rough hypoplastic amelogenesis imperfecta (AI) phenotype and to evaluate whether craniofacial variables are related to a mutation in either of the two genes associated with AI, enamelin (ENAM) and amelogenin (AMGX). Eight children (five males and three females) with rough hypoplastic AI phenotype, aged 6.5-15 years, from...

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 Amelogenin
Share to Dental Enamel Proteins

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to DNA Mutational Analysis

Share to Facies

Share to Pedigree

Share to Sequence Deletion

Share to Statistics, Nonparametric

Source

Identifiers

PMID: 21068190
DOI: 10.1093/ejo/cjq089

Genes

ENAM

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Craniofacial characteristics and genotypes of amelogenesis imperfecta patients.PMID 21068190Read ↗

Variation in dental and skeletal open bite malocclusion in humans with amelogenesis imperfecta.Semantic proximity Read ↗

Association between malocclusions and amelogenesis imperfecta genotype and phenotype: A systematic review.Semantic proximity Read ↗

Dental management of amelogenesis imperfecta patients: a primer on genotype-phenotype correlations.Semantic proximity Read ↗

Craniofacial structure related to inheritance pattern in amelogenesis imperfecta.Semantic proximity Read ↗

Clinical and radiographic findings of 125 cases with amelogenesis imperfectaSemantic proximity Read ↗

The molecular etiologies and associated phenotypes of amelogenesis imperfecta.Semantic proximity Read ↗

A nomenclature for X-linked amelogenesis imperfecta.Semantic proximity Read ↗

Amelogenesis imperfecta: an introduction.Semantic proximity Read ↗

The genetics of amelogenesis imperfecta: a review of the literatureSemantic proximity Read ↗

Amelogenesis imperfecta.Semantic proximity Read ↗

Amelogenesis Imperfecta; Genes, Proteins, and PathwaysSemantic proximity Read ↗

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

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