Chromosomes.
Chromosomes.
Asymptomatic carrier, a person or organism infected with an infectious disease agent, but displaying no symptomsGenetic carrier, a person or organism that has inherited a genetic trait or mutation, but displaying no symptoms
An individual who has inherited a factor for a trait is a carrier of that trait. They may or may not exhibit the trait themselves, as it depends on whether the inherited factor is dominant or recessive.
describe how you can use information about inherited traits to make health decisions
Albinism is a recessively inherited disease. People with albinism has inherited 2 albinism genes. They got one gene from each parent.
The carrier signal occurs at the beginning to transmit information.
No, thyroid hormones like T3 and T4 are primarily transported in the blood bound to carrier proteins such as thyroxine-binding globulin (TBG), transthyretin (TTR), and albumin. These carrier proteins help to maintain stable levels of thyroid hormones in the bloodstream and protect them from rapid clearance.
carrier is constant frequency information is a change from that constant
A carrier is a person who has inherited a genetic mutation but does not necessarily display the associated trait or disease. Carriers can pass on the mutation to their offspring.
The gene for haemophilia is located on the X chromossome, and can be passed by haemophiliac or carrier mothers to sons (more common) or daughters. Haemophiliac fathers will always have carrier (but not necessarily affected daughters.)
False.