Answer:
Answered below.
Explanation:
A karyotype is defined as the size, shape, and number of chromosomes present in an organism.
An analysis is usually done on a karyotype to see if individuals have abnormal numbers or sizes of chromosomes. Such abnormalities may arise from;
Deletion: which implies that a chromosomal part is missing.
Duplication: where parts of a chromosome are repeated.
Translocation: which occurs when a chromosomal part breaks off and gets attached to another chromosome.
Nondisjunction: in which chromosomes do not separate from the parent cells.
Common chromosomal disorders arising from these abnormalities include;
Down's syndrome
Edwards syndrome
Turner's syndrome
Klinefelter syndrome
Prada-willi syndrome
Cri-du-chat syndrome
Patau's syndrome
DNA is unzipped by helicase at the origin of replication. There are several origins of replications in eukaryotic DNA replication, while only one in prokaryotic replication.
<span>B. The have been Earth's only hominine for the last 24,000 years.
After the unknown eradication of the Homo Neanderthals, Homo Sapiens became the only homonine for the last 24,000 years. That is to say, that modern humans are the result of the evolution of homo sapiens to homo sapiens sapiens.</span>
a. 25%
b.75%
c. 50%
d. Male cats have only one X chromosome in their DNA meaning that they should be unable to inherit different colours.
