Human Biology (MindTap Course List)
11th Edition
ISBN: 9781305112100
Author: Cecie Starr, Beverly McMillan
Publisher: Cengage Learning
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Textbook Question
Chapter 20, Problem 7SQ
A gamete affected by nondisjunction could have __________.
- a. a change from the normal chromosome number
- b. one extra or one missing chromosome
- c. the potential for a genetic disorder
- d. all of the above
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Select the letter of the choice that best completes the statement. An extra chromosome can cause a defect known as trisomy 21 ora. Cooley’s anemia.b. Huntington’s disease.c. Down syndrome.d. PKU.
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Chapter 20 Solutions
Human Biology (MindTap Course List)
Ch. 20 - Prob. 1RQCh. 20 - What is a carrier of a genetic trait?Ch. 20 - What evidence indicates that a trait is coded by a...Ch. 20 - Prob. 4RQCh. 20 - Explain what nondisjunction is, and give two...Ch. 20 - _______ segregate during ______. a. Homologues;...Ch. 20 - Prob. 2SQCh. 20 - Genes on the same chromosome tend to stay together...Ch. 20 - Prob. 4SQCh. 20 - A chromosomes structure can be altered by _______....
Ch. 20 - Nondisjunction can be caused by ________. a....Ch. 20 - A gamete affected by nondisjunction could have...Ch. 20 - Genetic disorders can be caused by __________. a....Ch. 20 - A person who is a carrier for a genetic trait...Ch. 20 - Prob. 10SQCh. 20 - If a couple has six boys, what is the probability...Ch. 20 - Human sex chromosomes are XX for females and XY...Ch. 20 - People with Down syndrome have an extra copy of...Ch. 20 - Prob. 4CTCh. 20 - Prob. 5CTCh. 20 - About 4 percent of people of Northern European...Ch. 20 - The following pedigree shows the pattern of...
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Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, biology and related others by exploring similar questions and additional content below.Similar questions
- Consanguinity is having offspring together who are blood-related. Their children have a higher risk of having a second child with an autosomal recessive condition A. Both statements are correct B. Both statements are incorrect C. Statement 1 is correct. Statement 2 is incorrect D. Statement 2 is correct. Statement 1 is incorrectarrow_forwardA couple has three children one of the has Cystic Fibrosis (autosomal recessive). If neither parent is affected. What is the probability that their next child will be a sick boy? a. ¼ b. ½ c. 1/8 d. 3/8 e. 1/16arrow_forwardA trait that is present in a male child but not in either of his parents is characteristic of inheritance. a. autosomal dominant b. autosomal recessive c. X-linked recessive d. It is impossible to answer this question without more informationarrow_forward
- Which of the following terms describes the process of homologous chromosomes failing to separate correctly during meiosis?A. Chromatid adhesion syndromeB. NondisjunctionC. AmetaphasiaD. Anti-anaphasearrow_forwardColorblindness is a recessive x-linked trait. Which genotype represents a male with normal vision? a. XNXN b. XYN c. XnY d. XNYarrow_forwardIdentify whether the following terms is related to either mitosis or meiosis or both. 1. Identify whether the following terms is related to either mitosis or meiosis or both. a. mitosis b. meiosis c. both 2. somatic cells/ body cells a. mitosis b. meiosis c. both 3. two genetically similar diploid cellsarrow_forward
- Hemophilia is a disease caused by a gene found on the X chromosome. Therefore, it is a sex-linked disease which is caused by the recessive allele. Suppose, a man with hemophilia marries a woman who is homozygous dominant for the trait. Predict the genotype of the man. (XH = normal; Xh= hemophiliac) * a. XH Y b. XHXh c. XhXh d. Xh Yarrow_forwardHemophilia is a disease caused by a gene found on the X chromosome. Therefore, it is referred to as a sex-linked disease. The recessive allele causes the disease. A man with hemophilia (xhy) marries a woman who is homozygous dominant (XHXH. A. Illustrate using a Punnett square the probability that their children will have the disease. B. Will any of their children have the disease? C. Predict the probabilities of their children having the disease.arrow_forwardWhat is it called when chromosomes fail to separate properly during meiosis? A. Nondisjunction B. Karyotype C. Chromosomal separation failure D. Inappropriate separation E. Karyokinesisarrow_forward
- which is male with small testes, enlarged breasts, The genotype XXY corresponds to and decrease in body hair. a. Turner syndrome O b. Triplo-X Oc. Klinefelter syndrome d. Jacob syndromearrow_forwardA man who is a carrier for cystic fibrosis marries a woman who is a carrier for cystic fibrosis. Respond to the question based upon this scenario. The couple in the above scenario has four children. How many of their children will have cystic fibrosis? a. one b. two c. it could be none to all of their children d. it depends whether they are male or femalearrow_forwarda male and a female are each heterozygous for both Cystic Fibrosis and Phenylketonurea, both of which are autosomal recessive disorders. What proportion of their children will: a. have neither condition b. will have either of the two diseases c. be carriers of at least one of these diseasesarrow_forward
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