Answer:
diploid
Explanation:
So humans have two homologous chromosome sets in each cell, meaning humans are diploid organisms.
The genetic fault that usually causes colour vision deficiency is passed on in what's known as an X-linked inheritance pattern.
This means:
1) it mainly affects boys, but can affect girls in some cases
2) girls are usually carriers of the genetic fault – this means they can pass it on to their children, but do not have a colour vision deficiency themselves
3) it's usually passed on by a mother to her son – the mother will often be unaffected as she'll normally just be a carrier of the genetic fault
4) fathers with a colour vision deficiency will not have children with the problem unless their partner is a carrier of the genetic fault
5) it can often skip a generation – for example, it may affect a grandfather and their grandson
6) girls are only affected if their father has a colour vision deficiency and their mother is a carrier of the genetic fault
Answer:
The answers are :-
1.What is the term that refers to the change that happens in a living organism because of a stimulus?
<u>c)</u><u> </u><u>stimulus</u>
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<u>d)</u><u> </u><u>dog barks when there are </u><u>fireworks</u><u>.</u>
3. The process by which living organisms stay the same.
<u>b)</u><u> </u><u>homeostasis</u>
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<u>c) It </u><u>divides</u>
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Research has demonstrated that neural stem cells have an impaired ability to differentiate into functional neurons when subjected to ethanol. They found out that treating cultured neural system impairs their ability to differentiate in functioning neurons. With this impairment it seems to be united with aberrant, dense methylation and loci which are active in normal tissue.