Red-green color blindness is caused by an X-linked recessive gene. In a family, the mother is a carrier of this gene while the father does not have the gene. What are the possible effects on their children?
Are there any options? If not, here's the cross you must use: \[XX ^{r} \times XY\] If the child is a male, then the male has 50% chance of inheriting RG Color blindness. This is because the child would get the Y allele from his father, then one of the X alleles from his mother. If the child is a female, then there is no chance of getting RG color blindness, but there is a 50% chance of being a CARRIER of the gene. This is because the father would donate one X allele, and the mother would donate one of hers.
The only way to get RG color blindness in this scenario is: If you are male - \[X ^{r}Y\] You can be a CARRIER (heterozygous) in this scenario: If you are female \[XX ^{r}\] So for males its 50% chance of getting RG color blindness. Females its 0% chance. You can be a carrier though, and that would be 50% chance if you're a female.
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