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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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Detalles Bibliográficos
Autores principales:	Gerreth, Karolina, Zaorska, Katarzyna, Zabel, Maciej, Nowicki, Michal, Borysewicz-Lewicka, Maria
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Springer Berlin Heidelberg 2017
Materias:	Original Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5748405/ https://www.ncbi.nlm.nih.gov/pubmed/28382465 http://dx.doi.org/10.1007/s00784-017-2115-1

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