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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 no: | Clin Oral Investig |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Springer Berlin Heidelberg
2017
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| Assuntos: | |
| Acesso em linha: | 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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