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Terms 12.1

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Term
Definition
sex chromosome   one of the pair of chromosomes that determine the sex of an individual  
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autosome   any chromosome that is not a sex chromosome  
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sex-linked trait   a trait that is determined by a gene found on one of the sex chromosomes, such as the X chromosome or the Y chromosome in humans  
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linked genes   one pair of genes that tend to be inherited together  
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chromosome map   a diagram of gene positions on a chromosome  
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map unit   in chromosome mapping, an increment of 1% in the frecquency of crossing-over  
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germ-cell mutation   mutation that occurs in an organism's gametes  
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somatic-cell mutation   a mutation that occurs in a body cell  
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lethal mutation   a gene or chromosomal mutation that influences the development of an organism in such a way that the organism can't survive  
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deletion   the loss of DNA from a chromosome  
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inversion   a reverse in the order of the genes, or chromosome segment, within a chromosome  
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translocation   the movement of a segment of DNA from one chromosome to another, which results in a change in the position of the segment  
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nondisjunction   the failure of homologous chromosomes to separate during meiosis 1 or the failure of sister chromatids to separate during mitosis or meiosis 2  
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point mutation   a mutation in which only one nucleotide or nitrogenous base in a gene is changed  
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substitution   a mutation in which a nucleotide or a codon in DN is replaced with a different nucleotide  
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frameshift mutation   a mutation, such as the insertion or deletion of a nucleotide in a coding sequence, that results in the misreading of the code during translation because of the change in the reading frame  
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insertion mutation   a mutation in which one or more nucleotides are added to a gene  
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Created by: Addaleigh
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