A case of de novo mosaic 18q21.3 deletion with a mild phenotype

Genet Couns. 2014;25(1):71-3.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Child, Preschool
  • Chromosome Deletion*
  • Chromosome Disorders* / genetics
  • Chromosome Disorders* / pathology
  • Chromosome Disorders* / physiopathology
  • Chromosomes, Human, Pair 18 / genetics
  • Developmental Disabilities / diagnosis
  • Developmental Disabilities / genetics
  • Humans
  • Male
  • Mosaicism*
  • Phenotype

Supplementary concepts

  • Chromosome 18 deletion syndrome