Genetics: Analysis and Principles
6th Edition
ISBN: 9781259616020
Author: Robert J. Brooker Professor Dr.
Publisher: McGraw-Hill Education
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Chapter 28, Problem 11CONQ
What is polygenic inheritance? Discuss the issues that make polygenic inheritance difficult to study.
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Chapter 28 Solutions
Genetics: Analysis and Principles
Ch. 28.1 - 1. Which of the following is an example of a...Ch. 28.1 - 2. Saying that a quantitative trait follows a...Ch. 28.2 - The variance is a. a measure of the variation...Ch. 28.2 - 2. Which of the following statistics is used to...Ch. 28.3 - 1. For many quantitative traits, genotypes and...Ch. 28.4 - A QTL is a __________ where one or more genes...Ch. 28.4 - 2. To map QTLs, strains are crossed that differ...Ch. 28.5 - 1. In a population of squirrels in North Carolina,...Ch. 28.5 - Prob. 2COMQCh. 28.5 - 3. One way to estimate narrow-sense heritability...
Ch. 28.6 - 1. For selective breeding to be successful, the...Ch. 28.6 - Prob. 2COMQCh. 28 - Give several examples of quantitative traits.How...Ch. 28 - 2. At the molecular level, explain why...Ch. 28 - 3. What is a normal distribution? Discuss this...Ch. 28 - 4. Explain the difference between a continuous...Ch. 28 - What is a frequency distribution? Explain how such...Ch. 28 - 6. The variance for weight in a particular herd of...Ch. 28 - Two different varieties of potato plants produce...Ch. 28 - 8. If , would you conclude that a positive...Ch. 28 - Prob. 9CONQCh. 28 - When a correlation coefficient is statistically...Ch. 28 - 11. What is polygenic inheritance? Discuss the...Ch. 28 - What is a quantitative trait locus (QTL)? Does a...Ch. 28 - 13. Let’s suppose that weight in a species of...Ch. 28 - Prob. 14CONQCh. 28 - 15. From an agricultural point of view, discuss...Ch. 28 - Many beautiful varieties of roses have been...Ch. 28 - 17. In your own words, explain the meaning of the...Ch. 28 - 18. What is the difference between broad-sense...Ch. 28 - The heritability for egg weight in a group of...Ch. 28 - In a fairly large population of people living in a...Ch. 28 - When artificial selection is practiced over many...Ch. 28 - 22. Discuss whether a natural population of wolves...Ch. 28 - 23. With regard to heterosis, is each of...Ch. 28 - Here are data for height and weight among 10 male...Ch. 28 - 2. The abdomen length (in millimeters) was...Ch. 28 - 3. You conduct an RFLP analysis of head weight in...Ch. 28 - 5. Let’s suppose that two strains of pigs differ...Ch. 28 - Prob. 6EQCh. 28 - In a wild strain of tomato plants, the phenotypic...Ch. 28 - The average thorax length in aDrosophilapopulation...Ch. 28 - 9. In a strain of mice, the average 6-week body...Ch. 28 - Prob. 10EQCh. 28 - 11. A danger in computing heritability values from...Ch. 28 - For each of the following relationships,...Ch. 28 - An animal breeder had a herd of sheep with a mean...Ch. 28 - The trait of blood pressure in humans has a...Ch. 28 - Discuss why heritability is an important...Ch. 28 - From a biological viewpoint, speculate as to why...Ch. 28 - 3. What is heterosis? Discuss whether it is caused...
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- Create a hypothetical person and situation as a real life example to illustrate your position. Who is this person? How old is this person? What chromosomal abnormalities does this person have? How does genetic testing and counseling make this person’s life better or worse? Ultimately, should your hypothetical person seek genetic counseling?arrow_forwardSUBJECT: GENETICS Topic: Polygenic Inheritance Question: Discuss possible presentation why a given family with 12 children, has 7 variations/differences in terms of height (contributing alleles like AABBCCDDEEFF, non-contributing alleles, aabbccddeeff)arrow_forwardwhat is the probability that a couple (both heterozygous for the same recessive mutation) will have two children with the disease if the couple plans to have four children in total?arrow_forward
- Is Miller Fisher syndrome hereditary?arrow_forwardA young lady requested pre-marital genetic counselling because her sister had died in infancy of gangliosidosis, an autosomal recessive disease. What is the risk that this young lady has similarly affected offspring? What advice should be given?arrow_forwardWhat is extra chromosomal inheritance? explain with an example.arrow_forward
- Discuss the differences among sex-influenced, sex-limited, andsex-linked inheritance. Give examples.arrow_forwardCystic Fibrosis (CF) is an autosomal recessive condition. Therefore, heterozygous (Cc) carriers do not display symptoms. Two parents who are carriers plan to start a family and you are a genetic counselor helping to advise them about their chances of having children affected by CF. a) Suppose the couple has 4 children, each one year apart. What is the probability that all 4 children will inherit CF? b) What is the probability that any 3 of their 4 children will not inherit CF, but 1 will be affected? c) What is the probability that their first child will not inherit CF, but the younger 3 children will inherit CF?arrow_forwardPropose the most likely mode of inheritance (autosomal dominant, autosomal recessive, or X-linked recessive) for the following pedigrees. Affected individuals are shown with filled (black)symbols.arrow_forward
- What is autosomal pattern of Mendelian inheritance.? What disorder is caused by this pattern on inheritance.arrow_forwardThere are several possible modes of inheritance through which traits can be inherited. The following pedigree charts represent four different inheritance patterns. Match each type of inheritance with the correct pedigree numbered above. (Use each number only once.)X-linked recessive X-linked dominant Autosomal recessive Autosomal dominantarrow_forwardTuberous Sclerosis (TS) is an autosomal dominant genetic disease characterized by seizures, mental retardation, autism, and benign tumors of the brain, heart, skin, and kidneys. The kidney tumors can also be malignant. This disease exhibits a wide range of severity, and only about 1/3 of the cases are inherited. Two different genes have been tightly linked to the disease in families where it is inherited. The remaining 2/3 appear to be due to mutations in one of the 2 genes as well. Overall it appears that 1/2 are caused by mutations in TSC1 and the other half by mutations in TSC2. A rat model for hereditary renal carcinoma (kidney cancer) has been found. Southern and Northern blot analysis of the TSC1 and TSC2 gene revealed no differences between these rats and normal rats. Not all the rats in the strain would get cancer but a significant proportion did and those were selected for and used in experiments. 1. a) What was detected by the Southern blots? (look this up, make your…arrow_forward
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