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Exploring GRHL3 polymorphisms and SNP-SNP interactions in the risk of non-syndromic oral clefts in the Brazilian population.

Camilla de Marchi Sanches AzevedoRenato Assis MachadoHercílio Martelli-JúniorSilvia Regina de Almeida ReisDarlene Camati PersuhnRicardo Della ColettaAna Lúcia Carrinho Ayroza Rangel
Published in: Oral diseases (2019)
Our results confirm the importance of GRHL3 and its interactions with previously NSOC-associated genes, including FAM49A, FOXE1, NTN1, and VAX1, in the pathogenesis of NSOC in the Brazilian population.
Keyphrases
  • genome wide
  • dna methylation
  • gene expression
  • genetic diversity
  • autism spectrum disorder