Mary Frances Lyon studied gene expression and developed the theory of X-chromosome inactivation, also called Lyonization, during the twentieth century in the United Kingdom. The Lyonization hypothesis proposes that, even though females have two X-chromosomes and males have only one, one X-chromosome in females is always randomly inactivated, which causes males and females to have the same level of X-chromosome gene expression. Prior to Lyon’s hypothesis, scientists understood that there must be a biological way to compensate for the difference in X-chromosomes in males and females, but they did not know the exact mechanism. To investigate the topic, Lyon studied coat color in mice, a trait influenced by genes on the X-chromosome. Her resulting hypothesis highlighted X-chromosome inactivation as a mechanism for controlling gene expression in females without altering their DNA sequence. Through her research, Lyon aided scientists in understanding X-linked disorders, which laid the foundation for the development of gene therapies designed to treat X-linked disorders that affect hundreds of thousands of people globally.