Human Heredity: Principles and Issues (MindTap Course List)
11th Edition
ISBN: 9781305251052
Author: Michael Cummings
Publisher: Cengage Learning
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Textbook Question
Chapter 6, Problem 10QP
An individual is found to have some tetraploid liver cells but diploid kidney cells. Be specific in explaining how this condition might arise.
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Chapter 6 Solutions
Human Heredity: Principles and Issues (MindTap Course List)
Ch. 6 - Genetics in Practice case studies are...Ch. 6 - Genetics in Practice case studies are...Ch. 6 - Analyzing Karyotypes 1. Originally, karyotypic...Ch. 6 - Given the karyotype shown at right, is this a male...Ch. 6 - A colleague e-mails you saying that she has...Ch. 6 - What are the two most commonly used methods of...Ch. 6 - Prob. 5QPCh. 6 - Discuss the following sets of terms: a. trisomy...Ch. 6 - What chromosomal abnormality can result from...Ch. 6 - Tetraploidy may result from: a. lack of...
Ch. 6 - A cytology student believes he has identified an...Ch. 6 - An individual is found to have some tetraploid...Ch. 6 - A spermatogonial cell undergoes mitosis before...Ch. 6 - A teratogen is an agent that produces nongenetic...Ch. 6 - As a physician, you deliver a baby with protruding...Ch. 6 - Variations in Chromosome NumberAneuploidy Describe...Ch. 6 - A woman gives birth to monozygotic twins. One boy...Ch. 6 - Assume that a meiotic-nondisjunction event causes...Ch. 6 - Prob. 17QPCh. 6 - What is the genetic basis and phenotype for each...Ch. 6 - The majority of nondisjunction events leading to...Ch. 6 - Prob. 20QPCh. 6 - If all the nondisjunction events leading to Turner...Ch. 6 - Identify the type of chromosomal aberration...Ch. 6 - Describe the chromosomal alterations and phenotype...Ch. 6 - A geneticist discovers that a girl with Down...Ch. 6 - Albinism is caused by an autosomal recessive...Ch. 6 - Fragile-X syndrome causes the most common form of...
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- What chromosomal abnormality can result from dispermy?arrow_forwardThe pedigree shown below was obtained for a rare kidney disease. Determine the mode of inheritance for this condition and state your reasoning for your answer.arrow_forwardDetermining a karyotype is an important clinical method for diagnosing genetic disorders. Explain why it is useful for diagnosing monosomies and trisomies.arrow_forward
- By not explaining the stages,Briefly explain the difference between mitosis and meiosis with reference to the parent cell and the final cells that will formarrow_forwardDescribe both the primary gene or protein defect and the resulting phenotype for the following diseases a) Cystic fibrosis, b) Gaucher's diseasearrow_forwardName the technique by which one can disorder any possible chromosomal ormetabolic disorders in foetus.arrow_forward
- identify and label the chromosomes number (1-22). also, identify if it is male or female by labeling the X and Y chromosomes (this may be normal or abnormal)arrow_forwardChromosome abnormalities can be structural or numerical. Enumerate at least 3 examples of each, giving the numerical or structural changes in the chromosomes.arrow_forwardWrite a note on mitosisarrow_forward
- If the proband (III-2) marries a carrier woman, what is the probability that they will have an affected son? affected daughter? (Please show complete solution. Thanks.)arrow_forwardWhat are the major differences between mitosis and meiosis? Explain this both in terms of the different steps of each event and with regards to the final products of each event. Remember to mention the events which are unique to meiosis and why they are significant.arrow_forwardAnalyze the karyotype shown. Indicate if it is a chromosomal male or achromosomal female. If the karyotype is normal, write the word normal under name or description. If the karyotype is abnormal, name or describethe disorder.arrow_forward
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