<span>The most appropriate response would be for the nurse to ask the patient about their current concerns. This allows for the patient to actually elucidate what he or she is feeling at the time and does not hamstring the provider into actually giving a set length of time that they feel the patient has left to live, which can vary greatly from person to person.</span>
6 chromosomes. This is because gametes are usually characterised as to having only half the number of chromosomes of the somatic cells.
This is done through meiotic division.
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None: Only those mutations that occur in the germ line and result in gametes will have a chance of being passed on to progeny. An alteration in DNA that occurs after conception.
Somatic mutations can occur in any of the body's cells except germ cells (sperm and egg) and are therefore not passed on to children. These alterations can (but not always) cause cancer or other diseases. Mutations in somatic cells are called somatic mutations. Because they do not occur in the cells that give rise to gametes, the mutation is not transmitted to the next generation sexually. Human somatic cells have 46 chromosomes: 22 pairs and 2 sex chromosomes that may or may not form a pair. This is the 2n or diploid condition. Human gametes have 23 chromosomes, each of 23 unique chromosomes, one of which is a sex chromosome. Somatic cells are the cells in the body other than sperm and eggs (called germ cells). In humans, somatic cells are diploid, meaning they contain two sets of chromosomes, one inherited from each parent. Mutations in a somatic cell occur in somatic cells and are transmitted by mitosis, resulting in cancer. However, mutations in a gamete are passed on by meiosis, resulting in mutated offspring. A genetic mutation occurs during DNA replication, and chromosomal mutations occur during meiosis.
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