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EDA mutation by exome sequencing in non-syndromic X-linked oligodontia.

Luciane MartinsRenato Assis MachadoD S AraujoP A GiovaniP D RebouçasL P RodriguesL S MofattoM M RibeiroL L CoutinhoR M Puppin-RontaniR D ColettaF H NocitiK R Kantovitz
Published in: Clinical genetics (2017)
Keyphrases
  • intellectual disability
  • single cell
  • copy number
  • gene expression
  • dna methylation