Overview
Chromosomal mutations are significant alterations in the structure or number of chromosomes, which can lead to various genetic disorders. These mutations can occur through duplications, deletions, or translocations, each having distinct effects on an organism's genetic makeup. Understanding these mu...
Key Terms
Example: Humans have 23 pairs of chromosomes.
Example: A mutation in the BRCA1 gene can increase breast cancer risk.
Example: Some cancers are caused by gene duplications.
Example: Cri du chat syndrome is caused by a deletion on chromosome 5.
Example: Chronic myelogenous leukemia is often caused by a translocation.
Example: Down syndrome is a genetic disorder caused by an extra chromosome 21.