Prenatal diagnosis of chromothripsis, with nine breaks characterized by karyotyping, FISH, microarray and whole-genome sequencing

Prenat Diagn. 2015 Mar;35(3):299-301. doi: 10.1002/pd.4456. Epub 2015 Feb 4.
No abstract available

Publication types

  • Case Reports
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Abnormalities, Multiple / diagnosis
  • Abnormalities, Multiple / genetics*
  • Adult
  • Chromosome Disorders / diagnosis
  • Chromosome Disorders / genetics*
  • Female
  • Genome
  • Humans
  • In Situ Hybridization, Fluorescence
  • Karyotyping
  • Oligonucleotide Array Sequence Analysis
  • Pregnancy
  • Prenatal Diagnosis
  • Sequence Analysis, DNA
  • Translocation, Genetic