
Human Heredity: Principles and Issues (MindTap Course List)
11th Edition
ISBN: 9781305251052
Author: Michael Cummings
Publisher: Cengage Learning
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Explain how mitotic recombination leads to the mosaic
condition termed twin spots.
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- A colleague e-mails you saying that she has identified an interesting chromosome variation at 21q13. In discussing this discovery with a friend who is not a cytogeneticist, explain how you would describe this location, defining each term in the chromosome address 21q13.arrow_forwardFigure 7.2 If a mutation occurs so that a fungus is no longer able to produce a minus mating type, will it still be able to reproduce? Figure 7.2 (a) In animals, sexually reproducing adults form haploid gametes from diploid germ cells. (b) Fungi, such as black bread mold (Rhizopus nigricans), have haploid-dominant life cycles. (c) Plants have a life cycle that alternates between a multicellular haploid organism and a multicellular diploid organism. (credit c fern: modification of work by Cory Zanker; credit c gametophyte: modification of work by Vlmastra/Wikimedia Commons)arrow_forwardWhat mechanisms are responsible for: (a) duplication of a chromosome segment; (b) generation of a Down syndrome individual; (c) a chromosome translocation; and (d) polyploidy?arrow_forward
- Identify the type of chromosomal aberration described in each of the following cases: a. loss of a chromosome segment b. extra copies of a chromosome segment c. reversal in the order of a chromosome segment d. movement of a chromosome segment to another, nonhomologous chromosomearrow_forwardTheodor Boveri predicted that malignancies would often be associated with chromosomal mutation. What lines of evidence substantiate this prediction?arrow_forwardPeople with Down syndrome have an extra copy of chromosome 21, for a total of 47 chromosomes. However, in a few cases of Down syndrome, 46 chromosomes are present. This total includes two normal-looking chromosomes 21, one normal chromosome 14, and a longer-than-normal chromosome 14. Interpret this observation. How can these individuals have 46 chromosomes?arrow_forward
- Compare meiotic anaphase I with meiotic anaphase II. Which meiotic anaphase is most similar to the mitotic anaphase?arrow_forwardAssume that a meiotic-nondisjunction event causes trisomy 8 in a newborn. If two of the three copies of chromosome 8 are absolutely identical, at what point during meiosis did the nondisjunction event take place?arrow_forwardAbnormalities in the number of X chromosomes tend to be milder than the same abnormalities in autosomes because of _______. a. deletions b. nonbomologous recombinat ion c. synapsis d. X inactivationarrow_forward
- A geneticist discovers that a girl with Down syndrome has a Robertsonian translocation involving chromosomes 14 and 21. If she has an older brother who is phenotypically normal, what are the chances that he is a translocation carrier?arrow_forwardIn the following diagram, designate each daughter cell as diploid (2n) or haploid (n).arrow_forwardFamilial retinoblastoma, a rare autosomal dominant defect, arose in a large family that had no prior history of the disease. Consider the following pedigree (the darkly colored symbols represent affected individuals): a. Circle the individual(s) in which the mutation most likely occurred. b. Is the person who is the source of the mutation affected by retinoblastoma? Justify your answer. c. Assuming that the mutant allele is fully penetrant, what is the chance that an affected individual will have an affected child?arrow_forward
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