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Relating to two alleles of a gene pair in a heterozygote that are both fully expressed. When alleles for both white and read are present in a carnation, for example, the result is a rad and white carnation
x chromosome
pedigree
heredity
incomplete dominance
codominant
genotype
homozygous
allele
Condition in which a trait in an individual is intermediate between the phenotype of its two parents (blended)
x chromosome
pedigree
heredity
incomplete dominance
codominant
genotype
homozygous
allele
The actual code that alleles or genes posses (eg. TT, Tt, or tt). The gene may or may not be expressed when you observe a living organism
x chromosome
pedigree
heredity
incomplete dominance
codominant
genotype
homozygous
allele
Transmission of genetic traits from parent to offspring
x chromosome
pedigree
heredity
incomplete dominance
codominant
genotype
homozygous
allele
In humans and other mammals a sex chromosome, two of which are normally present in female cells and only one in male cells
x chromosome
pedigree
heredity
incomplete dominance
codominant
genotype
homozygous
allele
Diagrams that are used to trace the inheritance of a specific trait, abnormality, or disease. Standard symbols are used to represent males, females, mating and offspring
x chromosome
pedigree
heredity
incomplete dominance
codominant
genotype
homozygous
allele
An alternate form of a gene for one trait.
x chromosome
pedigree
heredity
incomplete dominance
codominant
genotype
homozygous
allele
A genotype consisting of two identical alleles of a gene for a particular trait
x chromosome
pedigree
heredity
incomplete dominance
codominant
genotype
homozygous
allele
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