A rare case of a de novo dup(19q) associated with a mild phenotype

J Med Genet. 2002 Oct;39(10):E61. doi: 10.1136/jmg.39.10.e61.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Child, Preschool
  • Chromosomes, Human, Pair 19 / genetics*
  • Developmental Disabilities / genetics
  • Female
  • Gene Duplication*
  • Humans
  • Phenotype