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Genetics and genomics etiology of nonsyndromic orofacial clefts.

Wasiu Lanre AdeyemoAzeez Butali
Published in: Molecular genetics & genomic medicine (2017)
Orofacial clefts (OFC) are complex birth defects. Studies using contemporary genomic techniques, bioinformatics, and statistical analyses have led to appreciable advances in identifying the causes of syndromic forms of clefts. This commentary gives an overview of the important cleft gene discoveries found using various genomic methods and tools.
Keyphrases
  • copy number
  • genome wide
  • intellectual disability
  • single cell
  • gene expression
  • case control
  • pregnant women
  • genome wide identification
  • genome wide analysis