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a type of cell division that results in four daughter cells each with half the number of chromosomes of the parent cell, as in the production of gametes and plant spores.\

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the analysis of DNA from samples of body tissues or fluids, especially when conducted in order to identify individuals.

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the haploid set of chromosomes in a gamete or microorganism, or in each cell of a multicellular organism.

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is an important component of every cell in the body.

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a unit of heredity that is transferred from a parent to offspring and is held to determine some characteristic of the offspring

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the number and visual appearance of the chromosomes in the cell nuclei of an organism or species.

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a threadlike structure of nucleic acids and protein found in the nucleus of most living cells, carrying genetic information in the form of genes.

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deoxyribonucleic acid, a self-replicating material present in nearly all living organisms as the main constituent of chromosomes. It is the carrier of genetic information.

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the passing on of physical or mental characteristics genetically from one generation to another.

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the record of descent of an animal, showing it to be purebred.

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the record of descent of an animal, showing it to be purebred.

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A particularly important category of genetic linkage has to do with the X and Y sex chromosomes

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is a form of dominance wherein the alleles of a gene pair in a heterozygote are fully expressed

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is a form of intermediate inheritance in which one allele for a specific trait is not completely expressed over its paired allele.

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Genes come in pairs, called alleles, and each pair is located in a specific position (or locus) on a chromosome.

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refers to having identical alleles for a single trait.

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most important, powerful, or influential.

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relating to or denoting heritable characteristics controlled by genes that are expressed in offspring only when inherited from both parents, i.e., when not masked by a dominant characteristic inherited from one parent.

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one of two or more alternative forms of a gene that arise by mutation and are found at the same place on a chromosome.

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is a cross between two different lines/genes that differ in two observed traits. In the Mendelian sense, between the alleles of both these loci there is a relationship of complete dominance - recessive.

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is a mating between two organisms with different variations at one genetic chromosome of interest

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: a square diagram that is composed of a grid of usually four boxes and is used to calculate and depict all the combinations and frequencies of the different genotypes and phenotypes among the offspring of a cross in accordance with Mendelian inheritance

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the extent to which something is probable; the likelihood of something happening or being the case.

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the set of observable characteristics of an individual resulting from the interaction of its genotype with the environment.

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the genetic constitution of an individual organism

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the study of heredity and the variation of inherited characteristics.