Array-CGH analysis in a patient with WAGR syndrome and a reciprocal translocation t(2;11) inherited from the normal father with double translocation

Am J Med Genet A. 2010 Aug;152A(8):2130-3. doi: 10.1002/ajmg.a.33517.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Chromosomes, Human, Pair 11 / genetics*
  • Chromosomes, Human, Pair 2 / genetics*
  • Comparative Genomic Hybridization*
  • Fathers
  • Humans
  • In Situ Hybridization, Fluorescence
  • Infant, Newborn
  • Male
  • Oligonucleotide Array Sequence Analysis*
  • Translocation, Genetic / genetics*
  • WAGR Syndrome / genetics*