A tandem duplication of chromosome 21 in a newborn showing a phenotype inconsistent with Down syndrome

Am J Med Genet A. 2010 Apr;152A(4):1043-5. doi: 10.1002/ajmg.a.33335.
No abstract available

Publication types

  • Case Reports
  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Pairing / genetics
  • Brain / abnormalities
  • Chromosome Aberrations*
  • Chromosomes, Human, Pair 21 / genetics*
  • Down Syndrome / genetics*
  • Female
  • Gene Duplication*
  • Genome, Human / genetics
  • Humans
  • Infant, Newborn
  • Karyotyping
  • Magnetic Resonance Imaging
  • Phenotype
  • Pregnancy