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Association of IFT88 gene variants with nonsyndromic cleft lip with or without cleft palate.

Amanda BarbaChristian UrbinaLorena MailiMatthew R GreivesSteven J BlackwellJohn B MullikenBrett ChiquetSusan H BlantonJacqueline T HechtAriadne Letra
Published in: Birth defects research (2019)
Our results suggest that variation in IFT88 may contribute to NSCLP risk, particularly in multiplex families from a non-Hispanic white population.
Keyphrases
  • copy number
  • genome wide
  • high throughput
  • african american
  • genome wide identification
  • dna methylation
  • transcription factor