Which of the following mutations cannot be inherited by a person's biological children? A mutation that the person inherited and is in all their cells A mutation that is in a gamete but none of the body cells A mutation that is in a body cell but none of the gametes

in humans, as well as with many other animals, sex is determined by special sex chromosomes. An individuai containing two X chromosomes is a female, while an individual possessing an X and Y chromosome is a male. The sex chromosomes bear alleles for traits. Sex linkage applies to genes that are located on the sex chromosomes. These genes are considered sex-linked because their expression and inheritance patterns differ between males and females. The genes present on the X chromosome are said to be X linked. Many more genes are present on the A chromosome than found on the Y chromosome. Nonetheless, those genes found on the Y chromosome are said to be Y linked. The Y chromosome is smaller than its homoloque, the X chromosome. Consequently, most of the loci present on the X chromosome are absent on the Y chromosome. 1. In humans, hemophilia is a sex linked trait. Females can be normal, carriers, or have the disease. Males will have the disease or not (but they won't be ever carriers) XH…

Edward’s syndrome in humans (trisomy 18) is characterized by which genetic feature? it involves a duplication of the entire genome it involves a deletion of one chromosome it involves a deletion of one gene it involves a duplication of one gene it involves a duplication of one chromosome

Hereditary hemochromatosis is an autosomal recessive genetic disorder that causes the body to absorb too much iron from the diet. This excess iron is stored in the body's tissues and organs, particularly the skin, heart, liver, pancreas, and joints. Because humans cannot increase the excretion of iron, excess iron can overload and eventually damage tissues and organs. Some individuals who are homozygous for this autosomal recessive gene experience only skin discoloration and joint pain, others experience heart disease in addition to the skin discoloration, still other individuals suffer also suffer from diabetes, severe heart disease, and liver damage. Name and define this genetic phenomenon and explain how it relates to this specific genetic situation described above.