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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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Shranjeno v:
Bibliografske podrobnosti
izdano v:Clin Oral Investig
Main Authors: Gerreth, Karolina, Zaorska, Katarzyna, Zabel, Maciej, Nowicki, Michal, Borysewicz-Lewicka, Maria
Format: Artigo
Jezik:Inglês
Izdano: Springer Berlin Heidelberg 2017
Teme:
Online dostop: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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