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Genetic and epigenetic studies in non-syndromic oral clefts.

Azeez AladeWaheed AwotoyeAzeez Butali
Published in: Oral diseases (2022)
The etiology of non-syndromic oral clefts (NSOFC) is complex with genetics, genomics, epigenetics, and stochastics factors playing a role. Several approaches have been applied to understand the etiology of non-syndromic oral clefts. These include linkage, candidate gene association studies, genome-wide association studies, whole-genome sequencing, copy number variations, and epigenetics. In this review, we shared these approaches, genes, and loci reported in some studies.
Keyphrases
  • copy number
  • genome wide
  • dna methylation
  • mitochondrial dna
  • case control
  • intellectual disability
  • genome wide association
  • autism spectrum disorder
  • transcription factor
  • single cell
  • human immunodeficiency virus