Human Anatomy & Physiology (11th Edition)
11th Edition
ISBN: 9780134580999
Author: Elaine N. Marieb, Katja N. Hoehn
Publisher: PEARSON
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15. The field of genetics that studies the mode of inheritance of complex or quantitative traits is called —————— genetics.
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- 5. Using skin color as an example of a multifactorial trait, explain why skin color produces a wide range of possible phenotypes within the human population.arrow_forward37. Look at this pedigree and circle each row yes/no. Any assumption (that is not outrageous) can be made) for example, can assume someone is a carrier.arrow_forward1. A new species of animal called the rekamriliob has been found in the wild. The lab you work in has been tasked with studying its genetics. So far, there have been 2 main phenotypes found in the wild. Through selective breeding, your lab has determined that the gene for purple color (P) is dominant to the gene for golden color (p). Another lab has determined that the thick limb trait is dominant to the thin limb variety. If you breed a purebred purple thick limbed rekamreliob male with a golden thin limbed female, you get 100% thick limed offspring that are purple in color. If you take two of these organisms and breed them together, please predict the following. Assume that rekameliobs lay an average of 32 eggs. The gametes produced if the genes are unlinked b. genes The expected numbers of the possible phenotype in the offspring with unlinked The gametes produced if the genes are linked (list all possibilities, and show which ones are the result of crossing over) d. List the…arrow_forward
- 1. Develop a micro-theme to include the following concepts: a. Differentiate between genetics and heredity b. Compare dominant and recessive traits c. Compare pure and hybrid offspringarrow_forward2. A pedigree of a rare disease associated with a mutation (deletion) in a genomie imprintedsutosomal gene is shown below. Individuals with the deletion and disease are shown in color,while those with the deletion but unaffected are indicated by dots. 1 2 I 1 2 II 1 2 3 4 III IV 1 3 4 5 8 V 2 5 8 9 12 13 14 15 1) What type of genomic imprinting is shown, why (1 point)? 2) Given that "A" to represent the normal allele and "A-" to represent the deletion allele, pleasespecify the possible genotype of the labeled individuals (4 points). (From I-1 to V-16,thirty-two in total. You need to distinguish the allele inherited from father and mother) 3) Explain the phenotype of IV-1, IV-2, V-3, V-11, and V-13. (3 points) 4) What is the probability that the offspring of V-5 will exhibit the disease? What about V-14?(2 points)arrow_forward4. You have two probes that detect RFLPS that are closely linked (that is, RFLP 1 and 2 tend to be passed on together). You have been asked to help settle a paternity case. The two possible fathers have the following RFLP pedigree. The child and mother are also probed with these two RFLP probes. Is one male more likely to be the father? If so, which one? Explain your reasoning. (The data below the pedigree are two Southern blots.) grandparents grandparents dad #1 dad #2 child mother Probe #1 Probe #2 ||arrow_forward
- 11. what is The statistic used to calculate the likelihood of genetic linkage between genes ?arrow_forwardAt the beginning of the 20th century, scientists argued whether DNA or protein would be the element of "inheritance?" a) Which molecule did they think would carry all the genetic information and why? b) Describe the contribution of Griffith, Avery et al., Hershey & Chase, and Watson and Crick in the field of genetics. Edit View Insert Format Tools Table 12pt v Paragraph v BI BIUA ev T v 目、 总 ..arrow_forward
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