Biology
Biology, 09.06.2020 10:57, emmaschloegl21x

In humans, oculocutaneous (OCA) albinism is a collection of autosomal recessive disorders characterized by an absence of the pigment melanin in skin, hair, and eyes. That is, normal pigmentation (A) is dominant over albinism (a). For this question, assume it is a single gene with two alleles. Assume it is a single gene with two alleles. If two people have normal pigmentation, what possible phenotypes may be observed in their offspring?

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In humans, oculocutaneous (OCA) albinism is a collection of autosomal recessive disorders characteri...

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