This would be probably true if the assumption that all possible genotypic variations would be equally distributed (so we would have 25% HH, 25% hh and 2x 25 Hh). If this distribution would be true and Huntingtons disease really was a single gene dominant trait diesase, then yes, we could expect such a distribution in the population.
Answer:
Nucleus
Explanation:
Humans are eukaryotic organisms. Their cells have a well-defined nucleus in which the genetic material is present in the form of chromosomes. Chromosomes have genes arranged in a linear manner. Genes represent the stretch of DNA that code for a specific protein. Being diploid organisms, humans have two complete sets of chromosomes. Therefore, each chromosome is present in pairs. These pairs are called homologous chromosomes. One chromosome of a pair comes from an egg cell and is called the maternal chromosome. The other chromosome is contributed by sperm and is called a paternal chromosome.
The pumping force of the ventricles moves blood through the arteries. The breathing movements exerts pressure on the chest veins, the valves in the larger veins keep the blood from flowing backwards, and the skeletal muscles' contraction all help the blood in veins to move.
It's very small so at the same speed to blood
