Spectral karyotyping, fluorescence in situ hybridization and molecular genetic analysis of de novo partial trisomy 7p (7p15.1 --> pter) and partial monosomy 9p (9p22 --> pter)

Prenat Diagn. 2005 Dec;25(12):1170-2. doi: 10.1002/pd.1300.
No abstract available

Publication types

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

MeSH terms

  • Abnormalities, Multiple / genetics
  • Chromosome Deletion
  • Chromosomes, Human, Pair 7*
  • Chromosomes, Human, Pair 9*
  • Female
  • Humans
  • In Situ Hybridization, Fluorescence / methods
  • Infant, Newborn
  • Monosomy / diagnosis*
  • Pregnancy
  • Pregnancy Outcome
  • Prenatal Diagnosis / methods*
  • Spectral Karyotyping / methods
  • Trisomy / diagnosis*