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Threadlike structures in the nuclei of cells that contain genetic material
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Chromosomes
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Group of compounds that provides a specific set of biochemical instructions
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Gene
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A complete set of genes that makes up a person's heredity
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Genotype
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Physical, behavioral, and psychological features that result from the interaction between one's genes and the environment
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Phenotype
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When both alleles in a pair of chromosomes are the same
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Homozygous
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When the alleles in a pair of chromosomes differ from each other
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Heterozygous
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Form of an allele whose chemical instructions are followed
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Dominant
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Allele whose instructions are ignored in the presence of a dominant allele
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Recessive
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Situation when one allele does not dominate another completely
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Incomplete dominance
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Disorder in which blood cells are misshapen and cannot pass through the body's smallest blood vessels
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Sickle-cell disease
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Disorder in which individuals have a dominant allele for normal blood cells and a recessive allele for sickle-shaped blood cells, resulting in mild anemia only in presence of oxygen deprivation
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Sickle-cell trait
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Inherited disorder in which the individual lacks a liver enzyme necessary to convert phenylaline (in dairy, bread, fish, and diet soda) into tyrosine, resulting in poisoning of the nervous system and mental retardation IF these foods are eaten
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Phenylketonuria (PKU)
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Fatal inherited disease characterized by progressive degeneration of the nervous system in middle age after developing normally through early adulthood, resulting in muscle spasms, depression, and significant changes in personality
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Huntingdon's disease
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Disorder caused by an extra 21st chromosome, resulting in mental retardation and distinguishable facial features such as upward slanting eyes, fold over the eyelid and flattened facial profile, and a life expectancy of 25 to 60 years. Advanced maternal age is a significant risk factor.
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Down Syndrome
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