Oculocutaneous Albinism is an inherited autosomal recessive condition caused by a mutation in the tyrosinase (TYR) gene. A male and female who are phenotypically normal, discover through genetic testing that they are both carriers of a TYR mutant allele. What is the probability that their first child will be biologically male and have Oculocutaneous Albinism? Select one: a. 1/8 b. 3/4 c. 1/4 d. 1/16 e. 1/2

Human Heredity: Principles and Issues (MindTap Course List)
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Author:Michael Cummings
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Chapter5: The Inheritance Of Complex Traits
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Oculocutaneous Albinism is an inherited autosomal recessive condition caused by a mutation in the tyrosinase (TYR) gene. A male and female who are
phenotypically normal, discover through genetic testing that they are both carriers of a TYR mutant allele. What is the probability that their first child will
be biologically male and have Oculocutaneous Albinism?
Select one:
а. 1/8
b. 3/4
c. 1/4
d. 1/16
e. 1/2
Transcribed Image Text:Oculocutaneous Albinism is an inherited autosomal recessive condition caused by a mutation in the tyrosinase (TYR) gene. A male and female who are phenotypically normal, discover through genetic testing that they are both carriers of a TYR mutant allele. What is the probability that their first child will be biologically male and have Oculocutaneous Albinism? Select one: а. 1/8 b. 3/4 c. 1/4 d. 1/16 e. 1/2
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