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any change in the nuvleotide sequence of a gene or chromosome
mutation
agent, such as radiation or a chemical substance, which causes mutation
mutagens
change in melanin, tyrosine
albinism
presence of different colored eyes in the same person
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often called "trisomy 21"/ extra chromosome on the 21st pair
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occur in gametes(sperm and egg) can be transmitted to offspring, give one example
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inherited blood disorder marked by flawed hemoglobin
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occur in other cells of the body little effect cannot be inherited example:
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aka chromosomal aberrations or alterations changes occured within the chromosome
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types of chromosomal mutation
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