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

Silvia Maitz, Barbara Gentilin, Anna Maria Colli, Tommaso Rizzuti, Emilia Brandolisio, Annalisa Vetro, Orsetta Zuffardi, Silvana Guerneri, Faustina Lalatta

Research output: Contribution to journalArticlepeer-review

Original languageEnglish
Pages (from-to)978-980
Number of pages3
JournalPrenatal Diagnosis
Issue number10
Publication statusPublished - Oct 2008


  • Array CGH
  • Chromosome 22q13.3 deletion
  • Congenital heart defect
  • Diaphragmatic hernia
  • FISH
  • Prenatal cytogenetics

ASJC Scopus subject areas

  • Genetics(clinical)
  • Obstetrics and Gynaecology

Cite this