Primary pulmonary dysgenesis in velocardiofacial syndrome: a second patient

Am J Med Genet A. 2003 Aug 30;121A(2):177-9. doi: 10.1002/ajmg.a.20142.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Chromosome Deletion
  • Chromosomes, Human, Pair 22
  • Craniofacial Abnormalities / diagnosis
  • Craniofacial Abnormalities / genetics
  • DiGeorge Syndrome / genetics
  • Female
  • Heart Defects, Congenital / genetics*
  • Humans
  • Immunologic Deficiency Syndromes / genetics*
  • Infant
  • Lung / abnormalities
  • Lung Diseases / physiopathology
  • Pulmonary Artery / abnormalities*
  • Syndrome