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Biology, 10.03.2020 00:23 nockturnal1993

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 albino characteristics.
For this question, assume the phenotype is determined by 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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