Answer:
<em>fragile X syndrome </em>
Explanation:
<em>FMR1 gene mutations</em><em> trigger fragile X syndrome.</em>The gene FMR1 offers instructions on how to make a protein called FMRP.
This gene helps to control the output of other proteins and plays a part in the growth of synapses that are specific nerve cell connections.
It creates a <em>variety of developmental issues including intellectual disabilities and cognitive impairment.</em> This disease usually affects males more significantly than women.
A carrier is a child who carries the genes of from parents but the gene doesn't show itself because of being masked by the dominant gene.
Answer:
A
Explanation:
its the one that makes more sense to me
Answer:
C) An inference is a prediction based on new knowledge that you acquire from research.
Eliminate.
Explanation:
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