In situ hybridization and translocation breakpoint mapping. II. Two unusual t(21;22) translocations

Cytogenet Cell Genet. 1985;39(3):173-8. doi: 10.1159/000132130.

Abstract

Using a combination of banding techniques, we examined two atypical 21;22 translocations, 46,XX or XY,t(21;22)(p11;q11). In situ chromosomal hybridization of a probe for the constant region of the lambda light chain locus demonstrated that the 22q11 breakpoints of both rearrangements were proximal to the C lambda gene cluster. These studies permitted us to distinguish the 22q11 breakpoints of these translocations from the breakpoint of the 22q--chromosome of chronic myelogenous leukemia.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Chromosome Banding
  • Chromosome Mapping
  • Chromosomes, Human, 21-22 and Y*
  • Female
  • Genes
  • Humans
  • Immunoglobulin Light Chains / genetics*
  • Immunoglobulin lambda-Chains / genetics*
  • Karyotyping
  • Lymphocytes / cytology
  • Nucleic Acid Hybridization
  • Translocation, Genetic*

Substances

  • Immunoglobulin Light Chains
  • Immunoglobulin lambda-Chains