Answer:
In strict mode, the narrow-sense heritability is the proportion of the additive genetic variance that contributes to the total of the phenotypic variance. This value can be associated with the inheritance of the a-thalassemia
.
Explanation:
A-thalassemia is a genetic disorder caused by mutations affecting four different genes that encode alpha-globin, thus affecting the hemoglobin production process and, consequently, oxygen transport. The mode of inheritance of the a-thalassemia may be associated with narrow sense heritability since the phenotype is manifested by gradation, i.e., each allele might contribute in similar mode to this genetic condition.
Enzymes are protein macromolecules.
<span>Conjugation in which two cells temporarily combine in order to transfer genetic materials. After combination they then divide again, allowing of the information to pass and replace the previous members of the population.</span>
Answer:
A.
Explanation:
When we say that an individual is <u>heterozygous</u>, it means that the two alleles at the locus we are studying are different from one another. That is, each one of the parents contributed a different allele.
On the other hand, If the alleles at that locus were the same we would say the individual is <u>homozygous</u>. In other words, the two parents contributed each the same type of allele.
