It is a rare genetic mutation that both the maternal and paternal partners have to be at least a carrier for the albinism gene.
Answer:
An autosomal dominant gene is one that occurs on an autosomal (non-sex determining) chromosome. As it is dominant, the phenotype it gives will be expressed even if the gene is heterozygous.
The chances of an autosomal dominant disorder being inherited are 50% if one parent is heterozygous (NL) for the mutant gene and the other is homozygous for the normal (NN), or 'wild-type', gene. This is because the offspring will always inherit a normal gene from the parent carrying the wild-type genes, and will have a 50% chance of inheriting the mutant gene from the other parent. If the mutant gene is inherited, the offspring will be heterozygous for the mutant gene, and will suffer from the disorder. If the parent with the disorder is homozygous for the gene, the offspring produced from mating with an unaffected parent will always have the disorder.
Explanation:
The answer would be D. Empiricality. Scientific Method can not, and will not deal with studies that are either for logic or for theism. This field may be beyond the scientific confirmability, meaning, it can not be proven by science, one example of this is the existence of a primary mover, or a God.
C) Occurs in areas without soil.
Primary succession occurs in lifeless areas in which <span>soil that is incapable of sustaining life is formed due to lava, sand dunes, and </span><span>rocks left from a retreating glacier.</span>