Study Guide for Campbell Biology
Study Guide for Campbell Biology
11th Edition
ISBN: 9780134443775
Author: Lisa A. Urry, Michael L. Cain, Steven A. Wasserman, Peter V. Minorsky, Jane B. Reece, Martha R. Taylor, Michael A. Pollock
Publisher: PEARSON
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Chapter 23, Problem 14TYK

Cystic fibrosis is a very serious genetic disorder that occurs in homozygotes for a recessive allele. Although the disease is extremely serious, this recessive allele appears with surprisingly high frequency in Caucasian populations. It has been suggested that siblings of individuals with cystic fibrosis may have some protection from certain bacterial infections of the gut. If this is true, then the recessive allele is maintained at high frequency by

  1. a. the founder effect.
  2. b. new mutations.
  3. c. heterozygote advantage.
  4. d. frequency-dependent selection.
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Why does sickle cell anemia remain more prevalent in Sub-Saharan Africa than in the rest of the world? a. Reduced access to medical facilities presidposes Sub-Saharan Africans to an increased chance od disease. b. The prevalence of malaria in Sub-Saharan Africa provided a selective advantage to individuals who were heterozygous. c. Infection with malaria provides a selective disadvantage to individuals who are heterozygous for the sickle cell allele. d. People of African ancestry are genetically predisposed to carry the sickle cell allele
Familial Mediterranean fever is an inheritable disorder that causes inflammation in the abdomen, chest, or joints. Let F be the dominant allele and let f be the recessive allele. The genotypes of individuals II-4, III-2, and IV-3, respectively, are Select one: a. F_, F_, and F_ b. F_, FF, and Ff c. Ff, F_, and Ff d. F_, Ff, and F_
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