A translocation 46,XY,t(1;2)(q32;q21) in a male with reproductive failure

Hum Genet. 1985;70(1):93. doi: 10.1007/BF00389470.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Humans
  • Male
  • Oligospermia / genetics*
  • Translocation, Genetic*