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Single suture craniosynostosis: Identification of rare variants in genes associated with syndromic forms. Am J Med Genet A. 2018 Feb;176(2):290-300.

C M ClarkeV T FokJ A GustafsonM D SmythA E TimmsC D FrazarJ D SmithC B BirgfeldA LeeR G EllenbogenJ S GrussR A HopperMichael L Cunningham
Published in: American journal of medical genetics. Part A (2018)
Keyphrases
  • intellectual disability
  • copy number
  • bioinformatics analysis
  • autism spectrum disorder