Craniosynostosis in the Ullrich-Turner syndrome

Am J Med Genet. 1991 Aug 1;40(2):252. doi: 10.1002/ajmg.1320400227.
No abstract available

Publication types

  • Case Reports
  • Comment
  • Letter

MeSH terms

  • Child
  • Craniosynostoses / genetics*
  • Female
  • Humans
  • Infant
  • Monosomy
  • Mosaicism
  • Turner Syndrome / genetics*
  • X Chromosome