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.
<h2>Plant cell:-</h2>
- plant cell have a well defined nucleus.
- plant cell have plastid.
- plant cell has a thick covering of wall.
- plant cells have many other organelles.
<h2>Prokaryotic cell:-</h2>
- prokaryotic cell has no nucleus.
- it do not have plastid.
- prokaryotic cell don't have any thick covering of wall or membrane.
- it has no organelles body.
The leaves of the plant compared to the plants around it are bigger because they are being token care of and watered and fed while the others take care of them selves also they are different types of plants :)
Those mutated genes are most commonly recessive. Females have two X chromosomes so they can have a chromosome with the mutated gene and one with the healthy gene. The healthy gene is dominant so the disease won't manifest, and the woman is only a carrier. Males have only one X chromosome and an Y chromosome. If they have the mutated gene on the X chromosome they won't have another X chromosome with the healthy gene.
To summarize, men can't be carriers and they only need one copy of the mutated X-linked gene while women need two copies of the mutated gene.
