Answer:
This definition suits that of "HOMOLOGOUS CHROMOSOMES"
Explanation:
Homologous chromosomes are similar pairs of chromosomes i.e. in length, gene positioning and centromere location (one from each parent) but not identical. Homologous chromosomes are not identical in the sense that, alleles on each pair may be different, resulting in genetic variation of the offspring.
Using humans as a case study, a karyotype (pictorial display of chromosomal arrangement) shows the complete set of chromosomes, which has two complete set (diploid). Each human cell contain 23 pairs of chromosomes, with each pair contributed by each parent i.e. 46 chromosomes in total. Every chromosome pair represents a set of homologous chromosome.
Hormones - they travel through the blood to other parts of the body. Hope This Helps!
Answer:
92 chromatids
Explanation:
During phosphate, the nuclear envelope of the cell (which is where the 92 chromatids are contained) begins to break down. The centrioles, which are the only present in animal cells, separate and each moves to an opposite end of the cell
Answer: Base pairs occur when nitrogenous bases make hydrogen bonds with each other.
Explanation: Each base has a specific partner: guanine with cytosine, adenine with thymine (in DNA), The hydrogen bonds are weak allowing it to "unzip"
