A prenatal case of duplication with terminal deletion of 5p not identified by conventional cytogenetics

Prenat Diagn. 2008 Dec;28(12):1171-3. doi: 10.1002/pd.2132.
No abstract available

Publication types

  • Case Reports
  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Abnormalities, Multiple / diagnosis
  • Abnormalities, Multiple / genetics
  • Chromosomes, Human, Pair 5*
  • Cytogenetic Analysis / methods
  • Female
  • Gene Deletion*
  • Gene Duplication*
  • Humans
  • Pregnancy
  • Prenatal Diagnosis / methods*
  • Young Adult