How does it contribute to genetic variation in humans

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Reference no: EM131092919

Please answer the following questions in a 200-word response minimum. Try your best to reference the text I will message you privately for how to access the text book. Or you can access it at this link (it may take some time to load): https://vk.com/doc257194956_437096191?hash=744dc3a08c6c00873f&dl=fdb9fff13f8ef8f1b1

1. According to your textbook, what are DNA, chromosomes, and genes? How are the terms similar? How are they different?

2. Choose TWO of the following topics. Define each of your choices and list some pros and cons involved with each. Try to use examples that you find interesting and/or current research in your responses as much as possible. (Choose 2 from below):

• the human genome project
• cloning of animals/humans
• DNA fingerprinting
• genetic engineering of plants
• stem cell research

3. How does the process of meiosis work? How does it contribute to genetic variation in humans?

Please use the link at Khan academy listed below to answer the question:

https://www.khanacademy.org/science/biology/cellular-molecular-biology

4. What is the purpose of DNA? How does it function in the process of cell division?

Please use the link at Khan academy listed below to answer the question:

https://www.khanacademy.org/science/biology/cellular-molecular-biology

5. On a related note, there are several genetic diseases/conditions related to people having an abnormal number of sex chromosomes (but they generally only have the physical organs of one sex). Some examples are X, XXX, XXXX, XXY, XYY, XXYY. (Notice there isn't a Y all by itself? That's because there are genes necessary for life found on the X chromosome, so humans can't live without an X.):

What are some of these conditions called and/or what are the symptoms that are expressed by individuals who have these genotypes? What causes them to happen?

Reference no: EM131092919

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