Prophase 1, where crossing over occurs and DNA is already replicated
Answer:
Man's genotype: XᴮY
Woman's genotype: XᴮXᵇ
Daughter's genotype: XᵇXᵇ
The daughter is not the man's child.
Explanation:
Color blindness is a sex-linked trait caused by a recessive allele located in the X chromosome (Xᴮ=normal vision; Xᵇ-color blind).
Women have two X chromosomes, while men have an X and a Y chromosomes. For that reason, women need to have two recessive alleles to be color blind, while men only need one Xᵇ to be colorblind.
Since the man has normal color vision, his genotype would be XᴮY.
If the daughter is her father's, she would have inherited his dominant Xᴮ allele, so she would have normal vision. However, she is colorblind, so her genotype is XᵇXᵇ. She is not the man's daughter.
The mother also has normal color vision, but her daughter inherited a recessive allele from her, so her genotype is heterozygous XᴮXᵇ.
The answer is the parafollicular cells :)
Answer:
If your just looking for a description here you go.
Explanation:
Most spiral galaxies contain a central bulge surrounded by a flat, rotating disk of stars. The bulge in the center is made up of older, dimmer stars, and is thought to contain a supermassive black hole. Approximately two-thirds of spiral galaxies also contain a bar structure through their center, as does the Milky Way.
Hope this helps.
What’s better then 24 25!
