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Article

Significance of genetic variations in developmental enamel defects of primary dentition in Polish children.

Clinical oral investigations - 1 Jan 2018

Gerreth Karolina, Zaorska Katarzyna, Zabel Maciej, Nowicki Michal, Borysewicz-Lewicka Maria

Abstract excerpt

OBJECTIVES: The aim of the study was to reveal the association between developmental defects of enamel (DDE) and single nucleotide polymorphisms (SNPs) in the ENAM, AMELX, AMBN, TUFT1, and TFIP11 genes. MATERIAL AND METHODS: The molecular analysis was carried out in 52 children, aged 10-42 months, from four nursery schools situated in the region of Poznan, Poland (26 individuals with hypomineralization and/or...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Open in PubMed Open full text

Identifiers

PMID: 28382465
DOI: 10.1007/s00784-017-2115-1
PMCID: PMC5748405

Genes

AMBN
AMELX
ENAM
TFIP11
TUFT1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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