Fetal Costello syndrome: description of phenotype of HRAS exon 1 mutations

Ultrasound Obstet Gynecol. 2020 Feb;55(2):274-275. doi: 10.1002/uog.20281.
No abstract available

Publication types

  • Letter
  • Research Support, Non-U.S. Gov't
  • Comment

MeSH terms

  • Abnormalities, Multiple* / genetics
  • Costello Syndrome* / diagnostic imaging
  • Costello Syndrome* / genetics
  • Exons / genetics
  • Humans
  • Mutation
  • Phenotype
  • Proto-Oncogene Proteins p21(ras) / genetics

Substances

  • HRAS protein, human
  • Proto-Oncogene Proteins p21(ras)