PRRX1 is mutated in a fetus with agnathia-otocephaly

Clin Genet. 2011 Mar;79(3):293-5. doi: 10.1111/j.1399-0004.2010.01531.x.
No abstract available

Publication types

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

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Abnormalities, Multiple / pathology
  • Adult
  • Animals
  • COS Cells
  • Chlorocebus aethiops
  • Female
  • Fetal Death / genetics
  • Gene Expression Regulation, Developmental
  • Heterozygote
  • Homeodomain Proteins / genetics*
  • Homeodomain Proteins / metabolism
  • Humans
  • Male
  • Mutation*

Substances

  • Homeodomain Proteins
  • PRRX1 protein, human