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33 Cards in this Set
- Front
- Back
Dominant Allele |
An allele that expresses its phenotypic effect even when heterozygous with a recessive allele |
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Recessive Allele |
An allele that produces its characteristic phenotype only when its paired allele is identical |
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Punnett Square |
A diagram that is used to predict an outcome of a particular cross or breeding experiment |
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Test Cross |
A genetic cross between a homozygous recessive individual and suspected heterozygote to determine the genotype of the unknown parent |
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Crossing Over |
The exchange of genes between homologous chromosomes, resulting in a mixture of parental characteristics in offspring. |
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Karyotype |
The number and visual appearance of the chromosomes in the cell nuclei of an organism or species. |
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Heterozygous |
Having two different alleles for a single trait. |
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Homozygous |
Having two of the same alleles for a single trait. |
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Gamete |
A mature haploid male or female germ cell that is able to unite with another of the opposite sex in sexual reproduction to form a zygote. |
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Allele |
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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Gene |
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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Meiosis |
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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Dihybrid Cross |
A cross between two different alleles that differ in two observed traits. Mendelian inheritance: relationship of completely dominant or completely recessive. |
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Monohybrid Cross |
A monohybrid cross is a mating between two individuals with different alleles at one genetic locus of interest. The character(s) being studied in a monohybrid cross are governed by two or multiple alleles for a single locus. (Completely dominant or completely recessive.) |
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Chromosome |
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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Gregor Mendel |
Augustinian monk and botanist whose experiments in breeding garden peas led to his eventual recognition as founder of the science of genetics (1822-1884) |
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Chromatid |
Each of the two threadlike strands into which a chromosome divides longitudinally during cell division. Each contains a double helix of DNA. |
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Centromere |
The point on a chromosome by which it is attached to a spindle fiber during cell division. |
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Spindle Fiber |
A protein structure that divides the genetic material in a cell. It is necessary to equally divide the chromosomes in a parental cell into two daughter cells during both types of nuclear division: mitosis and meiosis |
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Pedigree |
A genetic representation of a family tree that diagrams the inheritance of a trait or disease though several generations. |
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Autosomal Inheritance |
Pertaining to a chromosome that is not a sex chromosome. |
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X-Linked Inheritance |
A mode of genetic inheritance by which a dominant or recessive gene is carried on the X chromosome. |
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Genetic Drift |
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Gene Flow |
Variation in the relative frequency of different genotypes in a small population, owing to the chance disappearance of particular genes as individuals die or do not reproduce. |
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DNA Fingerprinting |
The analysis of DNA from samples of body tissues or fluids in order to identify individuals. |
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Genetic Cloning |
Process in which a gene of interest is located and copied (cloned) out of DNA extracted from an organism. |
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Genetic Engineering |
The deliberate modification of the characteristics of an organism by manipulating its genetic material. |
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Selective Breeding |
The process of selecting particular phenotypic traits (characteristics) by choosing which animal or plant males and females will sexually reproduce and have offspring together. |
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Translocation |
A chromosome abnormality caused by rearrangement of parts between non-homologous chromosomes |
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Nondisjunction |
The failure of one or more pairs of homologous chromosomes or sister chromatids to separate normally during nuclear division |
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Complete Dominance |
The dominant allele completely masks the effect of the allele that is recessive |
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Incomplete Dominance |
The dominant allele incompletely masks the effect of the allele that is recessive, resulting in a blended phenotype |
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Codominance |
Neither allele is dominant over the other; both alleles of a gene pair in a heterozygote are fully expressed. |