Definition(s)
- The
transfer of DNA sequences between two homologous genes, most often by unequal
crossing over during meiosis; can be a mechanism for mutation if the transfer
of material disrupts the coding sequence of the gene or if the transferred
material itself contains one or more mutations
-
Definition from: GeneReviews
from the University of Washington and the National Center for Biotechnology Information
See also Understanding Medical Terminology.