Malignancy in chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome)

Am J Med Genet A. 2006 Apr 15;140(8):906-9. doi: 10.1002/ajmg.a.31199.
No abstract available

Publication types

  • Case Reports
  • Letter
  • Research Support, N.I.H., Extramural
  • Review

MeSH terms

  • Child
  • Child, Preschool
  • Chromosome Deletion*
  • Chromosomes, Human, Pair 22 / genetics*
  • DiGeorge Syndrome / diagnosis
  • DiGeorge Syndrome / genetics*
  • Diagnosis, Differential
  • Female
  • Humans
  • Infant
  • Infant, Newborn
  • Male
  • Neoplasms / diagnosis
  • Neoplasms / genetics*
  • Velopharyngeal Insufficiency / diagnosis
  • Velopharyngeal Insufficiency / genetics*