Answer:
- person’s <u>genotype</u> is their unique sequence of DNA. More specifically, this term is used to refer to the two alleles a person has inherited for a particular gene. <u>Phenotype</u> is the detectable expression of this genotype – a patient’s clinical presentation.
Explanation:
person’s phenotype results from the interaction between their genotype and their environment.
The connection between genotype and phenotype is not always clear-cut. This means that you may encounter disparities between your patient’s genomic test result and their clinical presentation. Similarly, the phenotype of patients with a given genetic condition may vary greatly even within families.
Answer:
A: A tool for showing possible alleles of offspring in a test cross
Explanation:
Punnet squares use the alleles of the parents to find possible alleles of their offspring.
Introduced to a habitat similar to their own introduced to a habitat different than their own outcompete native species generally have no native predators generally have native predators often have high reproductive rates often have low reproductive rates can tolerate a range of conditions
Answer:
It is NOT D
Explanation:
On edge, the answer is NOT weathering
