Codominance is a type of inheritance in which both alleles of a gene are expressed in the phenotype of a heterozygote. This means that neither allele is dominant over the other, and both alleles contribute to the phenotype of the individual.

Blood type AB is an example of codominance because both the A and B alleles are expressed in the phenotype of the individual. This results in the individual having type AB blood.

An individual with codominant alleles has a heterozygous genotype. This means that they have one copy of the dominant allele and one copy of the recessive allele.

The phenotype of an individual with codominant alleles is a blend of the two phenotypes. This means that both alleles are expressed in the phenotype, and neither allele is dominant over the other.

Codominance is a type of inheritance in which both alleles of a gene are expressed in the phenotype of a heterozygote. This means that neither allele is dominant over the other, and both alleles contribute to the phenotype of the individual. Therefore, the genotype of an individual with codominant alleles cannot be homozygous dominant.

The probability of an offspring inheriting both dominant alleles from their parents is 25%. This is because each parent has a 50% chance of passing on the dominant allele, and the offspring must inherit one dominant allele from each parent in order to express the dominant phenotype.

The probability of an offspring inheriting both recessive alleles from their parents is 25%. This is because each parent has a 50% chance of passing on the recessive allele, and the offspring must inherit one recessive allele from each parent in order to express the recessive phenotype.

The probability of an offspring inheriting one dominant allele and one recessive allele from their parents is 50%. This is because each parent has a 50% chance of passing on the dominant allele and a 50% chance of passing on the recessive allele, and the offspring can inherit either combination of alleles.

The genotype ratio of a cross between two heterozygous individuals is 1:2:1. This means that there will be one offspring with the homozygous dominant genotype, two offspring with the heterozygous genotype, and one offspring with the homozygous recessive genotype.

The phenotype ratio of a cross between two heterozygous individuals is 3:1. This means that there will be three offspring with the dominant phenotype and one offspring with the recessive phenotype.

Eye color in humans is an example of incomplete dominance because the heterozygous genotype results in an intermediate phenotype. This means that the offspring of parents with different eye colors will have an eye color that is a blend of the two parents' eye colors.

An individual with incomplete dominant alleles has a heterozygous genotype. This means that they have one copy of the dominant allele and one copy of the recessive allele.

The phenotype of an individual with incomplete dominant alleles is an intermediate phenotype. This means that the phenotype is a blend of the two phenotypes, and neither allele is dominant over the other.

Incomplete dominance is a type of inheritance in which both alleles of a gene are expressed in the phenotype of a heterozygote. This means that neither allele is dominant over the other, and both alleles contribute to the phenotype of the individual. Therefore, the genotype of an individual with incomplete dominant alleles cannot be homozygous dominant.

The probability of an offspring inheriting both dominant alleles from their parents in a cross between two heterozygous individuals is 25%. This is because each parent has a 50% chance of passing on the dominant allele, and the offspring must inherit one dominant allele from each parent in order to express the dominant phenotype.