Biology: The Dynamic Science (MindTap Course List)
4th Edition
ISBN: 9781305389892
Author: Peter J. Russell, Paul E. Hertz, Beverly McMillan
Publisher: Cengage Learning
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Textbook Question
Chapter 49, Problem 2TYK
Which of the following processes does not increase genetic diversity?
a. parthenogenesis
b. random DNA mutations
c. genetic recombination
d. independent assortment
e. random combinations of paternal and maternalchromosomes
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One of the forms of rickets is inherited in the autosomal dominant way. This disease is a result of:
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O b. Changes in the number of chromosomes.
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e. Gene mutations.
O d. Polyploidy.
2) A. Explain how polyribosomes form.
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deletion of a single base pair?
C. Compare and contrast mitosis and meiosis with respect to their genetic outcomes?
D. What are the possible consequences of non-disjunction during cell division?
E. How does meiosis increase genetic diversity in populations?
In genetic maternal effect, the phenotype of the individual is determined by which of these statements?
A. The sex of the parent who transmits the gene
B. The nuclear genotype of the maternal parent
C. The sex of the individual with only one sex able to express the phenotype
D. Cytoplasmic genes usually located in the mitochondria
E. A combination of environmental factors and the genotype of the individual
Chapter 49 Solutions
Biology: The Dynamic Science (MindTap Course List)
Ch. 49.1 - Prob. 1SBCh. 49.2 - What are egg coats, and what is their function?...Ch. 49.2 - Prob. 2SBCh. 49.3 - Outline the roles of follicle-stimulating hormone...Ch. 49.4 - How does the oral contraceptive pill prevent...Ch. 49 - Prob. 1TYKCh. 49 - Which of the following processes does not increase...Ch. 49 - Prob. 3TYKCh. 49 - Prob. 4TYKCh. 49 - The slow block to polyspermy: a. is caused by a...
Ch. 49 - Prob. 6TYKCh. 49 - Prob. 7TYKCh. 49 - Prob. 8TYKCh. 49 - Prob. 9TYKCh. 49 - Prob. 10TYKCh. 49 - Prob. 11TYKCh. 49 - Prob. 12TYKCh. 49 - Prob. 13TYKCh. 49 - Prob. 14TYKCh. 49 - Prob. 15TYKCh. 49 - Prob. 16TYKCh. 49 - Prob. 17TYKCh. 49 - Prob. 18TYKCh. 49 - Prob. 1ITDCh. 49 - Prob. 2ITDCh. 49 - Prob. 3ITD
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- The chromosomal theory of inheritance states that genes are on chromosomes. Therefore, any chromosomal abnormality will affect the number and location of genes therefore lead to the over- and under- expression of genes. Which of the following condition will NOT result in the over-expression of a gene? A. Trisomy 18 B. Triploidy 3n C. Monosomy X D. Duplication of a chromosome segmentarrow_forwardAny deviation in the number of chromosomes that involves individual chromosomes, as opposed to entire sets of chromosomes, is known as which one of the following?a. Aneuploidy c. Duplication b. Disomy d. Translocationarrow_forwardWhich of the following is associated with chemical modifications to chromosomes that label alleles as coming from the mother or father? a. Multiple alleles b. Extranuclear inheritance c. Epigenetic marks d. Small non coding RNAsarrow_forward
- What biological mechanism allows humans with an XXX genotype to be healthy individuals? Group of answer choices A. haplodiploidy B. epistasis C. X inactivation D. small size of the Y chromosome E. small size of the X chromosomearrow_forwardA patient has mental deficiency, a short stature, and the mongolian type of the eyelid fold. The microscopical examination of the patient's karyotype revealed the presence of trisomy on the 21-st chromosome. What do we call the disease which is caused by this chromosomal abnormality? Select one: a. Down's syndrome. b. Klinefelter's syndrome. O c. Turner's syndrome. d. Edward's syndrome. e. Patau syndrome.arrow_forwardWhen one examines the pattern of inheritance of a trait and finds that it is transmitted from fathers to sons to grandsons (never appearing in the females genotype) what is the conclusion about the inheritance pattern? a. Sex linked b. Sex limited С. Sex related d. X linked e. Sex influenced Red-Green color blindness a. Has its genetic determination on the x chromosome b. Affects more males than females С. Is influenced by somatic sex differentiation d. A and b e. All of thesearrow_forward
- The following image shows one specific stage of meiosis. Which of the following correctly states what is occurring in this stage? A. Microtubules have begun to pull sister chromatids apart, pulling them toward the poles of the cells. There are two cells at this stage. B. Microtubules have begun to pull homologous chromosomes apart, pulling them toward the poles of the cell. There is only one cell at this stage. C. Microtubules have attached to the chromosomes. Homologous chromosomes are aligned at the midpoint of the cell. There is only one cell at this stage. D. The chromosomes have reached the poles of the cell. There are technically two cells, but cytokinesis has begun in each.arrow_forwardWhich of the following is a TRUE statement regarding the outcome of meiosis? A. In meiosis, one diploid cell (2n) can produce 2 haploid cells in males (1n). B. In meiosis, four haploid cells (1n) can produce 2 diploid cells (2n) in males. C. In meiosis, one diploid cell (2n) can produce up to 4 haploid cells (1n) in males. D. In meiosis, one diploid cell (2n) can produce 2 diploid cells (2n) in females.arrow_forwardWhat can you assert regarding cytoplasmic inherited traits? A. extensive phenotypic variation exhibited, even within a single family B. reciprocal crosses that give different results C. All of the answers are correct. D. usually inherited from one parent, typically the maternal parent E. present in both males and femalesarrow_forward
- How many chromosomes are there in the somatic cells of a newborn boy with: a. The cri-du chat syndrome b. Klinefelter syndrome c. Down syndrome due to a 14/21 Robertsonian translocation d. Triploidy e. Edwards syndromearrow_forwardDuring the observation of a baby the diagnosis of Down's syndrome was made. What is the main cause of this pathology? Select one: a. Trisomy on the 13-th chromosome. b. Trisomy on the 21-st chromosome. c. Trisomy on X chromosome. d. Monosomy on the 1-st chromosome. O e. Undivergence of sex chromosomes.arrow_forwardWhich of the following meiotic events by itself does NOT result in an abnormal set of genes in a gamete? a. Translocation b. Deletion c. Nondisjunction d. Recombination e. Inversionarrow_forward
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