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Biology, 12.02.2020 04:49, nanagardiner08
Blood type is characterized by the combination of alleles that an individual has at two different loci. Three alleles (I A, IB, and i) encode ABO blood group antigens. There are two co-dominant alleles (LM and LN) encode another set of antigens, the MN blood group (homozygous LM individuals have type M, homozygous LN individuals have type N, and heterozygous LMLN individuals have type MN). For the crosses below, what is the probability that a child will have a unique blood genotype (at BOTH loci) that is not the same as the blood group genotypes of either parent?
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