Answer:
A parent with one copy of a dominant allele and one recessive coded Ww for the widow's peak is called heterozygous for a trait and has a 50 percent chance of passing on the dominant allele to each of his or her offspring, regardless of the gene inherited from the other parent.
Explanation:
hope this helps in some way sorry if it does not
The aorta carries oxygen rich blood away from the heart.
The pulmonary artery transports deoxygenated blood from the heart to the lungs.
The inferior vena cava carries deoxygenated blood from the lower body to the heart.
The coronary artery branches from the aorta and provide oxygen to the heart muscles.
Answer:
Pleiotropy
Explanation:
Pleiotropy is a genetic condition in which a single gene conditions the expression of multiple phenotype. There are different types of pleiotropy depending on the underlining mechanism
- <em>gene pleiotropy</em>
- <em>developmental pleiotropy</em>
- <em>selectional pleiotropy</em>
- <em>antagonistic pleiotropy </em>
<em>Phenylketonuria is a disease characterized by increased level of amino acid phenylalanine in the blood. It caused by mutation to the gene responsible for breaking down phenylalanine in the blood. Elevated level of phenylalanine causes other issues such as mental problems, urine coloration and reduction in skin pigmentation. This is a clear case of pleiotropy.</em>
Answer b
I think I’m not sure
Explanation:
It is expected to see in the offspring of a woman who has DMD and a man who does not have the disease that all of their sons and none of their daughters will have the disease
Option A.
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Explanation:</u></h3>
Duchene muscular dystrophy, also known as DMD is a recessive, x-linked disease. It occurs when there is a mutation in the dystrophin gene. This mutation further affects the muscles of the body leading it to degenerate and ultimately death.
When a woman with DMD and a man without DMD have an offspring, their daughters and the sons will get the mutated gene signature from the mother as she is the carrier. But since the father has normal genes, the daughters will become the carriers and will not be afflicted by it. This is because the normal X chromosome from the father will be passed on to them. The sons on the other hand will have the disease as they will get one of their mother's X chromosome which would be carrying the mutated gene.
