Answer:
(d) At least one child is phenotypically normal.
Step-by-step explanation:
To be a carrier means that you have the gen but you are not affected by it.
If both parents have that recessive gene, this means, both are heterozygous for that trait.
Let's say this gen is A, for the dominant trait, and "a" if it's recessive.
The mother and the father are Aa.
If you cross them you have Aa x Aa = AA Aa aA aa
This means you have 50% of Aa, carrier children
25% AA, not a carrier or affected by this gen.
25% aa, affected by the gen.