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Biology, 11.02.2020 01:11 bayl3ighh

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. If both parents display the albino phenotype, 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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