GENETICS(LL)-W/CONNECT >CUSTOM<
GENETICS(LL)-W/CONNECT >CUSTOM<
6th Edition
ISBN: 9781260571561
Author: HARTWELL
Publisher: MCG CUSTOM
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Chapter 15, Problem 15P

Why are severe mitochondrial or chloroplast gene mutations are usually found in heteroplasmic cells instead of homoplasmic cells?

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What is heteroplasmy? How it affects mitochondrial inheritance? Use specific examples to describe your results?
Are mutations that arise during mitosis or meiosis the same? Explain in 15 sentences.
Cystic fibrosis is a disease that occurs when an individual carries two copies of a recessive version of a membrane transport gene. A person that is a carrier for cystic fibrosis (that means they carry one copy of the gene that causes cystic fibrosis but their other copy is normal - they do not have cystic fibrosis) has a child with another person that is also a carrier for cystic fibrosis. What is the probability that this couple has three children that do not have cystic fibrosis AND are also not carriers of cystic fibrosis? 0.25 0.422 0.016 2.25 0.75

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GENETICS(LL)-W/CONNECT >CUSTOM<

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