A carrier of a genetic disorder who does not show symptoms is most likely to be heterozygous for the trait and able to transmit it to offspring. This particular individual has inherited a recessive allele for a genetic trait or mutation but does not display that trait or show symptoms of the disease. They are referred to as genetic carriers. The chance of two carriers having an offspring with the disease or genetic disorder is 25%
The determining factors are; climate, environment, and Human Activity.
P.S.: try those...lmk if they are right ;)
This is known as double helix. Nucleotides each have three parts: phosphate, sugar molecule<span>, and one of four </span>bases<span>. The </span>bases<span> include: A, (adenine), g (guanine), t (thymine), c (cytosine). ... </span>Explain why complementary base pairing is necessary to maintain the double helix shape of the DNA molecule<span>.</span>