This document presents information on complementation tests. It defines complementation tests as a method used to determine if two mutations are in the same gene or different genes. It explains that if the mutations are complementary (in different genes), the offspring will show the parental phenotypes, but if they are not complementary (in the same gene), the offspring will show a new phenotype. Three examples of using complementation test results to determine the number of genes involved are provided. The document concludes by citing a reference for more information on assigning mutations to genes using complementation tests.