Chromosome 22q11.2 deletion syndrome

Pediatr Rev. 2015 Jun;36(6):270-2; discussion 272. doi: 10.1542/pir.36-6-270.
No abstract available

MeSH terms

  • DiGeorge Syndrome* / diagnosis
  • DiGeorge Syndrome* / genetics
  • DiGeorge Syndrome* / therapy
  • Humans
  • Phenotype