Answer :
a) Chromosomal translocation is the process by which duplicated gene sequences have gotten from one chromosome to another.
In the field of biology, chromosomal translocation can be described as a process in which the genes of one chromosome have the ability to jump to another chromosome. A portion of genes break from the original chromosomes and move to another chromosome during the process of chromosomal translocation.
This is the reason that the genes responsible for the synthesis of globin molecules are present on chromosome 11 as well as chromosome 16. Multigene families are formed as a result of the process of chromosomal translocation.
Although a part of your question is missing, you might be referring to this question:
Multigene families include two or more nearly identical genes or genes sharing nearly identical sequences. A classical example is the set of genes for globin molecules, including genes on human chromosomes 11 and 16. How might identical and obviously duplicated gene sequences have gotten from one chromosome to another?
a) chromosomal translocation
b) chromosomal mutation
c) induction process
d) none of the above
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