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.
Answer:
Where is the experiment performed and the graph
Petit-mal seizure
Petit mal seizure is a form of
epilepsy with short sudden, unannounced lapses in consciousness. Impairment of
consciousness is the essential symptom. The sufferer experiences loss of
consciousness for 10 to 30 seconds, eye or muscle flutterings and a loss of
muscle tone.
