A simplified method for the detection of Y chromosome microdeletions in infertile men using a multiplex sequence-tagged site-based amplification

Genet Test. 2002 Fall;6(3):207-10. doi: 10.1089/109065702761403379.

Abstract

Sixteen sequence-tagged sites (STSs) were combined in five amplification reactions, to screen for deletions of DNA fragments located within the AZFa, AZFb, and AZFc regions of the Y chromosome. This multiplex strategy is fast and reliable, and most of the azoospermia-associated deletions reported so far are detected with this simplified method. Internal control STSs are included that allow discrimination between deletion and failure of amplification.

MeSH terms

  • Base Sequence
  • Chromosomes, Human, Y*
  • Humans
  • Infertility, Male / genetics*
  • Male
  • Sequence Deletion*
  • Sequence Tagged Sites*