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Significance of genetic variations in developmental enamel defects of primary dentition in Polish children
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, f...
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| Publicado en: | Clin Oral Investig |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Springer Berlin Heidelberg
2017
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5748405/ https://ncbi.nlm.nih.gov/pubmed/28382465 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00784-017-2115-1 |
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