Refining the critical region of the novel 19q13.11 microdeletion syndrome to 750 Kb

J Med Genet. 2009 Jun;46(6):421-3. doi: 10.1136/jmg.2009.066910.
No abstract available

Publication types

  • Comment
  • Letter

MeSH terms

  • Child, Preschool
  • Chromosome Deletion*
  • Chromosomes, Human, Pair 19 / genetics*
  • Humans
  • Male
  • Syndrome