ABSTRACT
The mode of action of sex-linked genes in mammals has been the subject of much discussion in recent years. This has centred round the concept that in the mammalian female, either the maternal or the paternal X-chromosome is randomly and irreversibly inactivated during development, with the result that in the female, as in the male, one X-chromosome only is active in a given cell (Lyon, 1966, and earlier papers). The Lyon Hypothesis (L.H.) is based, in part, on the mottled or striped phenotypes of heterozygotes for certain sexlinked genes affecting the coat of the mouse and other mammals: these phenotypes are regarded as a mixture of clones descended from cells in which either one or the other X-chromosome has been inactivated. As Baker (1967) rightly insists, the interpretation of a pattern as clonal must be based on known cell lineages, as without such a basis one simply postulates what should be put to the test.