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genetics 2

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Term
Definition
chromosome theory of inheritance   the theory that genes are carried fro parents to offspring  
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genes   segmants of DNA found in chromosomes that are passed from one generation to the next  
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DNA   a genetic material that determines inherited characteristics  
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genetic disorder   an abnormal condition that a person inherits through genes or chromosomes  
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mutations   are changes in the DNA of genes of chromosomes. affects genetic info  
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sex chromosomes   determine if your a boy or a girl  
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hemophilia   genetic disorder, slows down the blood clotting after getting cut.  
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insertation   a mutation when an extra base is added to a DNA strand  
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deletation   when a base is left out of the DNA strand  
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substitution   the wrong base is used in a DNA strand  
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carrier   an individual who inherited an altered form of a gene but had no effects or symptoms of that gene or mutation  
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mutations that dont harm or benefit you   eye color, birth marks  
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mutations that are harmful   sickle-cell anemia, down syndrome  
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mutations that are beneficial   immune to malaris and HIV  
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down syndrome   47 chromosomes instead of 46  
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cystic fibrosis   body pruduces toomuch mucus in the lungs and intesines  
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sickle-cell disease   affects the production of hemoglobin in the blood. causes blocked blood vessels  
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karyotype   a map of all the chromosomes in the cell. the chromosomes ar earanged in pairs  
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pedigree   chart or "family tree" that tracks which members of afamily have that particular trait  
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selective breeding   breeding organisoms with desired traits so that their offspring will have those traits  
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inbreeding   crossing 2 identical organisims for that exact look  
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hybridization   breeding 2 genetically different individuals (2 different species)  
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genetic engeneering   a technique to produce organisoms with desired traits  
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fertilization   the act of fertilizing an egg  
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Created by: madison_sherer
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