Expanding the phenotype of 22q13.3 deletion: report of a case detected prenatally

Prenat Diagn. 2008 Oct;28(10):978-80. doi: 10.1002/pd.2110.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Chromosome Deletion*
  • Chromosomes, Human, Pair 22 / genetics*
  • Female
  • Fetal Heart / abnormalities
  • Humans
  • Phenotype
  • Pregnancy
  • Prenatal Diagnosis*
  • Young Adult