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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Vydáno v:Clin Oral Investig
Hlavní autoři: Gerreth, Karolina, Zaorska, Katarzyna, Zabel, Maciej, Nowicki, Michal, Borysewicz-Lewicka, Maria
Médium: Artigo
Jazyk:Inglês
Vydáno: Springer Berlin Heidelberg 2017
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Original Article
On-line přístup: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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