Xeroderma pigmentosum (XP) is an autosomal recessive condition characterized by moderate to severe sensitivity to ultraviolet (UV) light. Patients develop multiple skin lesions on UV-exposed skin, and skin cancers often develop as a result. XP is caused by deficient repair of DNA damage from UV exposure. Many genes are known to be involved in repair of UV-induced DNA damage, and several of these genes are implicated in XP. What genetic phenomenon is illustrated by XP?