Hint
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Answer
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One of two or more versions of DNA sequence (a single base or a segment of bases) at a given genomic location.
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A
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Allele
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Any chromosome that is not a sex chromosome.
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A
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Autosome
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A person who can pass an inherited (genetic) disease on to their children but who does not have the disease.
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C
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Carrier
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A threadlike structure made of protein and a single molecule of DNA that serves to carry the genomic information from cell to cell.
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C
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Chromosome
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A type of inheritance in which two versions (alleles) of the same gene are expressed separately to yield different traits in an individual.
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C
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Co-dominance
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A condition wherein the dominant allele completely masks the effect of the recessive allele.
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C
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Complete dominance
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A type of mutation in which part of the DNA sequence is lost; the loss can be as small as a single base pair or as much as an entire section of a chromosome.
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D
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Deletion
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A cell having two complete sets of chromosomes; one set is inherited from the mother, and one set from the father.
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D
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Diploid cell
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The common name of deoxyribonucleic acid, the molecule that carries genetic information for the development and functioning of an organism; made of two linked strands that wind around each other to resemble a twisted ladder — a shape known as a double helix.
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D
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DNA
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(of an allele) When the alleles of a gene are different, the allele that is expressed.
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D
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Dominant allele
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The basic physical and functional unit of heredity.
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G
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Gene
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The complete set of genetic information in an organism.
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G
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Genome
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The alleles or variants an individual carries in a particular gene or genetic location.
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G
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Genotype
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Having inherited different versions (alleles) of a genomic marker from each biological parent.
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H
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Heterozygous
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Having inherited the same versions (alleles) of a genomic marker from each biological parent.
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H
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Homozygous
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A form of gene interaction in which both alleles of a gene at a locus are partially expressed.
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I
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Incomplete dominance
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A mutation that causes premature the death of an organism, often in the early stages of embryonic or fetal development, but sometimes after birth.
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L
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Lethal mutation
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A specific, fixed position on a chromosome where a particular gene or genetic marker is located.
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L
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Locus
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Membrane-bound organelles that generate most of the chemical energy needed to power the cell’s biochemical reactions.
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M
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Mitochondria
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An individual's observable traits as determined by their genomic makeup and environmental factors.
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P
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Phenotype
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(of an allele) Having no tangible effect, or that is masked by the effects of a dominant allele.
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R
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Recessive
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The common name of Ribonucleic Acid, a single-stranded organic molecule composed of nucleotides.
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R
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RNA
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A specific characteristic of an individual, determined by genes, environmental factors or by a combination of both.
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T
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Trait
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A gene that resides on the X chromosome.
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X
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X-linked gene
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The single cell formed by the union of gametes (sperm and egg); a fertilized egg.
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Z
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Zygote
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