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 journalArticle

Original languageEnglish
Pages (from-to)978-980
Number of pages3
JournalPrenatal Diagnosis
Volume28
Issue number10
DOIs
Publication statusPublished - Oct 2008

Keywords

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

ASJC Scopus subject areas

  • Genetics(clinical)
  • Obstetrics and Gynaecology

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