The correct answer is option B.
Genotype AA, Phenotype-Unaffected.
How did this occur ?
- The cystic fibrosis is a condition caused by the inheritance of the two recessive allele, It is an autosomal recessive disease.
- In the given case, the parents are carriers, and the carriers are always heterozygotes.
- Hence, the phenotype of the both parent should be Aa. A possible cross of the parents is shown in the figure below.
- In case, the progeny have a single dominant trait, the child would not be affected, but will be a carrier and can pass the disease to offspring.
- In case, the child inherit both the dominant allele (homozygous dominant) from the parents, then he/she would be unaffected. In case, the phenotype of the child is homozygous recessive then it would be affected.
To know more about Genotype from the given link
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