Klinefelter syndrome is an consequence of what type of mutation?
a. deletion
b. insertion
c. frame shift
d. nondisjunction

b. insertion

The Klinefelter syndrome is caused by an insertion mutation. It occurs when there is an existence of an excess or extra X chromosome in each cell that may cause an abnormality in the development of males. It usually affects the physical and cognitive development of male with symptoms varying from one person to another.  Kids with these type of disorder may experience  learning disabilities and even speech and language  problems.  These kids tend to be quiet and very sensitive. They can also be very passive.

I’m not exactly sure what your trying to ask, but if it’s how an organelle is similar to a body system or a part a nucleus is like a in function. but i don’t fully understand what you’re trying to ask