Answer:
0%
Explanation:
This involves a single gene coding for melanin pigment in the skin. The recessive form of this gene (allele) is albinism while the dominant form is a normal skin. The question highlights that the normal male parent (dominant) has no family history of albinism, this means that nobody in their family has ever possessed albinism or has been a carrier/heterozygous for the trait. This is because a carrier/heterozygote will always produce the recessive trait (albinism) if crossed with another carrier or albino individual.
In a nutshell, the normal male parent is homozygous for the dominant trait. Hence, if a homozygous dominant male is crossed with an albino woman (homozygous recessive), all their offsprings will possess a heterozygous genotype and dominant phenotype. Meaning that none of their children will ba an albino.
Hence, the percentage of their child being an albino is 0.
Answer:
At the microscopic level of a visceral muscle cell are actin and myosin filaments. They slide past each other in an antiparallel manner to shorten the distances between their ends. In a smooth muscle cell, the ends of chains of these functional units are attached to the cell membrane. They are several in a cell arranged in an elaborate framework. They contract together and deferentially to enable the muscle to contract as needed.
Answer: Pulmonary aortic valve
Explanation:
Embryonic Skin Cells is the correct answer.
<span>Hope this helps, and Brainliest answer would be appreciated!</span>
Answer:
harmful effect and no effect
Explanation:
No effect: most mutated genes destroy themselves before it gets to far
Harmful effect: an example of harmful effects would be down-syndrome (where you have 3 21-chromosomes and you are only supposed to have 2)
