Screening for celiac disease in patients with deletion 22q11.2 (DiGeorge/velo-cardio-facial syndrome)

Am J Med Genet A. 2003 Sep 1;121A(3):286-8. doi: 10.1002/ajmg.a.20254.
No abstract available

Publication types

  • Letter

MeSH terms

  • Abnormalities, Multiple / diagnosis
  • Abnormalities, Multiple / genetics*
  • Adolescent
  • Celiac Disease / diagnosis
  • Celiac Disease / genetics*
  • Child
  • Child, Preschool
  • Chromosome Deletion*
  • Chromosomes, Human, Pair 22 / genetics*
  • DiGeorge Syndrome / diagnosis
  • DiGeorge Syndrome / genetics*
  • Face / abnormalities
  • Female
  • Humans
  • Male
  • Phenotype
  • Velopharyngeal Insufficiency / genetics