Inquiry Into Life (16th Edition)
16th Edition
ISBN: 9781260231700
Author: Sylvia S. Mader, Michael Windelspecht
Publisher: McGraw Hill Education
expand_more
expand_more
format_list_bulleted
Concept explainers
Videos
Textbook Question
Chapter 23, Problem 7A
Which of the following does not have an autosomal recessive pattern of inheritance?
- Cystic fibrosis.
- Huntington disease
- Phenylketonuria
- Sickle cell disease
- None of these are correct
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solution
Students have asked these similar questions
Which of the following disorders in humans has an autosomal dominant inheritance pattern?
Hemophilia
Albinism
Tay-Sachs disease
Huntington’s disease
What type of inheritance is shown in the
pedigree?
sex linked recessive
autosomal recessive
sex linked dominant
autosomal dominant
What is the mode of inheritance shown here?
Sex-linked recessive
Autosomal recessive
Autosomal dominant
Sex-linked dominant
Chapter 23 Solutions
Inquiry Into Life (16th Edition)
Ch. 23.1 - Describe how Mendel's law of segregation and law...Ch. 23.1 - Define the term allele, and explain what it means...Ch. 23.1 - Contrast genotype and phenotype, and use...Ch. 23.1 - Predict outcome ratios and probabilities for...Ch. 23.1 - Prob. 1QTCCh. 23.1 - 2. Decide the reasons listed in the feature, what...Ch. 23.1 - Prob. 3QTCCh. 23.1 - Distinguish between the terms genotype and...Ch. 23.1 - Explain the purpose of testcross.Ch. 23.1 - Prob. 3CYP
Ch. 23.1 - Describe the types of process that result in a 3:1...Ch. 23.2 - Recognize autosomal dominant and autosomal...Ch. 23.2 - Analyze pedigree to determine the probability of a...Ch. 23.2 - Describe the characteristics of a Pedigree for an...Ch. 23.2 - Prob. 2CYPCh. 23.3 - Prob. 1LOCh. 23.3 - Prob. 2LOCh. 23.3 - Describe polygenic inheritance.Ch. 23.3 - What would be the potential consequences if one of...Ch. 23.3 - Prob. 2QTCCh. 23.3 - Prob. 1CYPCh. 23.3 - Prob. 2CYPCh. 23.4 - Prob. 1LOCh. 23.4 - Understand how scientists determine the effect of...Ch. 23.4 - Prob. 1CYPCh. 23.4 - Prob. 2CYPCh. 23 - Prob. C2BYBCh. 23 - Prob. S5.4BYBCh. 23 - Prob. S5.6BYBCh. 23 - The law of segregation states all of the following...Ch. 23 - Prob. 2ACh. 23 - Prob. 3ACh. 23 - Prob. 4ACh. 23 - Prob. 5ACh. 23 - Prob. 6ACh. 23 - Which of the following does not have an autosomal...Ch. 23 - 8. Which of the following does not describe the...Ch. 23 - Prob. 9ACh. 23 - Prob. 10ACh. 23 - Prob. 11ACh. 23 - Prob. 12ACh. 23 - Prob. 1TCCh. 23 - How would you determine whether a disease in...Ch. 23 - Prob. 3TC
Knowledge Booster
Learn more about
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
- Cystic Fibrosis Cystic fibrosis is an autosomal recessive disorder that affects 1 in 3 000 newborns with Caucasian background. It causes thick mucus build-up in various organs and can cause damages and problems in respiratory and digestive systemsarrow_forwardWhich of the following mode of inheritance most likely to representthe pedigree showing the pattern of inheritance of a rare disorder? Autosomal dominant X linked dominant Autosomal recessive X linked recessivearrow_forwardOne of your patients, a six-year-old girl who suffers from Sickle cell anemia, an inherited blood disorder in which red blood cells are abnormally shaped and fragile, leading to a short supply of red blood cells. These abnormal cells can also get stuck in small vessels, which prevent blood flow, leading to fatigue, pain and other severe complications. Sickle cell anemia is an autosomal recessive disorder. Neither of your patient's parents has sickle cell anemia. What is the most likely genotype of her parents? (The normal beta-globin allele is abbreviated as B, and the abnormal allele as b.) one is B and one is b one is BB and one is bb both are Bb both are bb both are BBarrow_forward
- Which of the following genetic disorders is described by the following: Recessive sex-linked disorder. More common in males. Results in the inability to distinguish some colors. Male-pattern baldness Cystic fibrosis albinism colorblindnessarrow_forwardPlease help me with the following question: Von Willebrand disease is an inherited bleeding disorder. People with von Willebrand disease take a much longer period for blood to clot/stop than others. von Willebrand disease is either inherited in an autosomal dominant pattern or in an autosomal recessive pattern. Question: what is the genotype of the disorder? what are the phenotypic effects of the disorder? What is happening with the DNA to cause the phenotypic effects?arrow_forwardWhich genotype indicates a carrier of an autosomal recessive trait? bb BB Bbarrow_forward
- Among the following, which inheritance pattern increases the occurrence of the disease? Autosomal dominant Sex linked dominant Mitochondrial O Autosomal recessivearrow_forwardGenetic Inheritance Patterms Retinitis pigmentosa (RP) can be autosomal recessive, autosomal dominant, or x-linked. Apparently the dominant forms are often less severe. Eric's form of RP is Usher's Syndrome, which is an autosomal recessive inheritance (i.e., you must get a copy of the defective gene from your Mom and one from your Dad). Autosomal means it is not carried on one of the chromosomes that determines sex. Usher's Type II is recessive, so for Eric this means that both his Mom and Dad are carriers of this condition. His brother, Dirk, does not have any symptoms of RP. Draw a pedigree of Eric's family showing possible genotypes and chances of having RP. Your pedigree must include his parents, Eric, his brother Dirk, and a potential daughter of Eric's. Draws a pedigree that shows the correct genotypes and chances of having retinitis pigmentosa for Eric and his family. D.Focus (United States) a S W 37 F 八 口arrow_forwardGenetic disorders Complete the following statements to describe several genetic disorders and their symptoms. Choices can be used more than once. The disorder called causes blue-colored skin, sickle-cell disease osteogenesis imperfecta The disorder called that leads to weakened, brittle bones. causes defective collagen methemoglobinemia autosomal dominant The disorder called causes abnormally thick mucus in the bronchial tubes and pancreatic ducts. autosomal recessive The disorder called leads to progressive cystic fibrosis degeneration of neurons in the brain. alkaptonuria The disorder called causes urine to be black. Huntington disease acer %23 24 & 4 8. 9. e y u < 6arrow_forward
- A couple are both phenotypically normal but their son suffers from hemophilla, a sex linked recessive disorder. What fraction of their children are likely to suffer from hemophilia. what fraction are likely to be carriers.arrow_forwardA woman with Huntington’s disease (autosomal dominant trait, and she is heterozygous) has children with a healthy man. What proportion of their children will inherit Huntington’s disease?arrow_forwardAn unaffected man and an unaffected woman mate and have a daughter affected with Fifimania. Which of the following mechanisms of inheritance can not be ruled out? Choose all that can not be ruled out. Autosomal Recessive Autosomal Dominant X-linked Dominant X-linked Recessive All of the mechanisms shown can be ruled out Y-linkedarrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
How to solve genetics probability problems; Author: Shomu's Biology;https://www.youtube.com/watch?v=R0yjfb1ooUs;License: Standard YouTube License, CC-BY
Beyond Mendelian Genetics: Complex Patterns of Inheritance; Author: Professor Dave Explains;https://www.youtube.com/watch?v=-EmvmBuK-B8;License: Standard YouTube License, CC-BY