WAGR syndrome with deletion of chromosome 11p11.2-13

J AAPOS. 2004 Aug;8(4):396-7. doi: 10.1016/j.jaapos.2004.05.008.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Aniridia / diagnosis
  • Cataract / congenital
  • Chromosome Deletion*
  • Chromosomes, Human, Pair 11 / genetics*
  • Humans
  • Infant, Newborn
  • Male
  • WAGR Syndrome / diagnosis
  • WAGR Syndrome / genetics*