It's A, sex linked traits can be carried by either X or Y chromosomes.
The population affected is females. The chromosome that this affects is on the X chromosome which is the sex chromosome that females carry. This affects 1 in every 2,500 live births.
In both males and females there are 22 perfectly matched chromosomes. The somatic cells in humans total 46 chromosomes. Females get the XX sex chromosome while males get the Y chromosome.
Yes, and males have an X and a Y chromosome.
In females, the extra X chromosome becomes inactive and becomes the Barr body.
Yes, although it has less DNA and is smaller than its partner the X chromosome
Nope! The disease is equally in both males and females. This means that it is autosomal.
Female transmit 23 chromosomes to the offspring. She has that unique chromosome called as X chromosome. This is transmitted to the offspring. From male you get either X or Y chromosome. From XX chromosome you get female child. From XY chromosome you get male child.
The sex chromosome typically carried by an ovum is X-chromosome. The sperm may carry either x or y sex chromosome.
Because the gene that causes hemophilia is located on the X chromosome, so it will occur in males more frequently than in females.
The gene for eye color is only carried on the X chromosome. Since females have two X chromosomes and white is recessive, there are no white-eye females.
Yes. It is found as a mutation on the X chromosome (a sex chromosome) so it is sex linked. The gene for Fragile X is carried on the X chromosome. Because both males (XY) and females (XX) have at least one X chromosome, both can pass on the mutated gene to their children.
individuals that are heterozygous for alleles
It is on the X Chromosome (male have XY chromosome Females have XX Chromosome)
The population affected is females. The chromosome that this affects is on the X chromosome which is the sex chromosome that females carry. This affects 1 in every 2,500 live births.
sex-linked inheritance
CGD is an X-linked genetic disease, meaning the defective gene is carried on the X chromosome (one of the sex chromosomes). Females have two copies of the X chromosome, whereas males have one X and one Y.
Overall, colorblindness is much more common in males than females due to the fact that it is a sex-linked trait. The gene for colorblindness is carried on the X chromosome. Since this is a recessive condition, males will be more likely to express it due to the fact they only have one X chromosome while the females have two.