Associated Papers
Amelogenesis imperfecta: Analysis of the genetic basis and treatment with a digital workflow: A clinical report.
Klein P et al.
The Journal of Prosthetic Dentistry, 2025
Genetic Screening of a Nonsyndromic Amelogenesis Imperfecta Patient Cohort Using a Custom smMIP Reagent for Selective Enrichment of Target Loci.
Hany U et al.
Human Mutation, 2025
Amelogenesis imperfecta: Next-generation sequencing sheds light on Witkop's classification.
Bloch-Zupan A et al.
Frontiers in Physiology, 2023
An Intron c.103-3T>C Variant of the AMELX Gene Causes Combined Hypomineralized and Hypoplastic Type of Amelogenesis Imperfecta: Case Series and Review of the Literature
Leban T et al.
Genes, 2022
A Novel AMELX Mutation, Its Phenotypic Features, and Skewed X Inactivation.
Duan X et al.
Journal of Dental Research, 2019
Amelogenesis Imperfecta; Genes, Proteins, and Pathways.
Smith CEL et al.
Frontiers in Physiology, 2017
Molecular analysis for genetic counselling in amelogenesis imperfecta.
Aldred MJ et al.
Oral Diseases, 2002
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