Achild has sickle-cell disease (ss) but neither parent is ill. what must be true of her parents’ genotypes? one parent has two recessive alleles. both parents are heterozygous carriers. the father is heterozygous; the mother is normal. the mother is heterozygous; the father is normal.

Both parents are heterozygous carriers.

Explanation: Since sickle cell disease is a recessive trait, it means the affected person will have "homozygous recessive" state of genotype only. Here parents are normal, which means they are carriers. So their genotype would be Ss, heterozygous.

Heterozygous parents only will have 25% chances of having their children affected.

Option 1 is incorrect, because if one parent has two recessive alleles, it means he/she is affected and this contradicts the situation mentioned in question.

Option 3 and 4 are incorrect because it is mentioned in question that both parents are normal.

hey bro i looked it up on google the structure of the eye-spot in euglena viridie, e. ehrenbergii, and phacus pyriyorme is not as franzé haa described it. the so-called “crystal body” and “lens bodies” were not found in any of the individuals of the species examined by me. as earlier observers have stated, the eye-spot consists simply of a mass of pigment granules arranged in a single layer, and probably embedded in a protoplasmic framework, but the latter could not be seen, and its presence was only inferred from the fact that the pigment granules must be held together in some way, thd the eye-spot as a whole is capable of expansion, and that the pigment granules can be separated from each other.

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