A 4q21-q22 deletion in a girl with severe growth retardation

Clin Genet. 2002 Mar;61(3):226-8. doi: 10.1034/j.1399-0004.2002.610311.x.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Child
  • Child, Preschool
  • Chromosome Deletion*
  • Chromosomes, Human, Pair 4*
  • Female
  • Growth Disorders / genetics*
  • Humans
  • In Situ Hybridization, Fluorescence
  • Karyotyping