Down syndrome with partial trisomy of chromosome 21 because of a de-novo unbalanced translocation t(13;21)(q10;q22)

Clin Dysmorphol. 2012 Oct;21(4):200-203. doi: 10.1097/MCD.0b013e32835909cc.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Chromosomes, Human, Pair 10 / genetics*
  • Chromosomes, Human, Pair 13 / genetics*
  • Chromosomes, Human, Pair 21 / genetics*
  • Down Syndrome / genetics*
  • Humans
  • In Situ Hybridization, Fluorescence
  • Infant
  • Karyotyping
  • Male
  • Translocation, Genetic*
  • Trisomy / genetics*