The scenario will be Son: 25% colorblind daughter: 25% colorblind son: 25% of carrier daughters with normal vision: 25% normal son
<h3>What is color blindness?</h3>
The condition is frequently inherited. Certain eye diseases and medications are also possible causes. Men are more affected than women.
Color blindness is characterized by the inability to distinguish between red and green shades.
A colorblind man's genotype is XcY, and a heterozygous carrier female's genotype is XcX. A cross between XcY and XcX would result in progeny with the following ratio=
Son: 25% colorblind daughter: 25% colorblind son: 25% of carrier daughters with normal vision: 25% normal son.
Thus, the couple is likely to have a son who is half normal and half affected. Similarly, the couple is likely to have 50% normal daughters and 50% colorblind daughters.
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Answer:
the fundamental unit of heredity
Explanation:
DNA is a double stranded helix structure. Each strand is made up of a string of nucleotides.
A gene is a region of DNA, usually tens of thousands of nucleotides long. At the simplest level, one gene encodes for one trait. Therefore, the gene can be described as the fundamental unit of heredity.
Genes work by coding for specific proteins, which carry out essentially all the functions in the cell.
I think it is
rock metamorphosis
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The correct answer is Turgor. Turgor pressure keeps plants rigid, that is why plants are called turgid.