Suppose we have a disease phenotype that is determined by a single gene with two alleles. Further suppose it follows a autosomal recessive mode of inheritance with reduced penetrance. We have an individual who is unaffected (does not have the disease phenotype) and whose genotype is unknown. We cross this individual with a true-breeding affected individual. How many possible genotypes can this unaffected individual have at the disease locus
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Suppose we have a disease phenotype that is determined by a single gene with two alleles. Further su...
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