Fluorescence in situ hybridization using the subtelomeric 11q probe as a diagnostic tool for congenital thrombocytopenia

Ann Hematol. 2006 Dec;85(12):883-5. doi: 10.1007/s00277-006-0177-2. Epub 2006 Sep 15.
No abstract available

Publication types

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

MeSH terms

  • Chromosome Aberrations
  • Chromosome Banding / methods
  • Chromosome Breakage
  • Chromosomes, Human, Pair 11
  • DNA Probes*
  • Female
  • Humans
  • In Situ Hybridization, Fluorescence / methods*
  • Infant, Newborn
  • Thrombocytopenia / congenital*
  • Thrombocytopenia / diagnosis*

Substances

  • DNA Probes