BIOL 1010/1020 CLASS ONLY CONNECT
14th Edition
ISBN: 9781260038644
Author: Mader
Publisher: MCGRAW-HILL HIGHER EDUCATION
expand_more
expand_more
format_list_bulleted
Concept explainers
Textbook Question
Chapter 23, Problem 2TC
How would you determine whether a disease in humans is simply polygenic or and environmental influence?
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solutionStudents have asked these similar questions
Why are recessive conditions more common than dominant ones? How could being a carrier of a recessive disease be beneficial?
Why are most genetic diseases caused by recessive alleles?
Recessive genetic disorders are more frequent than disorders inherited as dominant because :
a) carriers are not eliminated by the disease before reproduction
b ) people carrying dominant genetic disorders always die before birth
c ) dominant genetic disorders are never expressed in males
e ) recessive genetic disorders are limited to persons of the same ethnicity
Chapter 23 Solutions
BIOL 1010/1020 CLASS ONLY CONNECT
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 - Prob. 2LOCh. 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 - 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 - Prob. 1CSCh. 23 - Prob. 2CSCh. 23 - Prob. 1ACh. 23 - Prob. 2ACh. 23 - Prob. 3ACh. 23 - Prob. 4ACh. 23 - Prob. 5ACh. 23 - Prob. 6ACh. 23 - Prob. 7ACh. 23 - Prob. 8ACh. 23 - Prob. 9ACh. 23 - Prob. 10ACh. 23 - Prob. 11ACh. 23 - Prob. 12ACh. 23 - Prob. 1AGPCh. 23 - Prob. 2AGPCh. 23 - Prob. 3AGPCh. 23 - Prob. 4AGPCh. 23 - Prob. 5AGPCh. 23 - Prob. 6AGPCh. 23 - Prob. 7AGPCh. 23 - Prob. 8AGPCh. 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
- Do people look differently upon those afflicted with mental illness if we have a perspective grounded in an understanding that this is a genetic diagnosis? How so?arrow_forwardWhy are the concepts of variable expressivity, incomplete penetrance, and delayed age of onset so important in relation to genetic diseases?arrow_forwardThe role of the TPMT genotype in response to treatment emphasizes the importance of pharmacogenomics. What changes in treatment would be recommended for someone homozygous recessive for TPMT, compared to someone that is homozygous dominant?arrow_forward
- Nancy Jones is a doctor who specializes in genetic diseases. For many years she has been studying populations of people who have Huntington’s disease. Dr. Jones has a special interest in Huntington’s disease because her mother died of this disease after many years living in a wheelchair. Dr. Jones’s father does not appear to have the disease. She has developed a test that can detect the dominant Huntington’s gene before symptoms appear and she has performed this test on many people. This test involves mapping a person’s genome to determine if the dominant Huntington’s gene is present. Dr. Jones is unsure if she should take the test herself as it will not prevent the disease from developing, only give the person advanced warning of the disease. Nancy Jones has a sister. Draw a pedigree chart that maps the disease through this family. Make sure to indicate those family members that have the disease, those that do not have the disease and those whose status is unknown. If you were Nancy…arrow_forwardHow does the physical storage of information in DNA influence the phenotype of an individual? Why does it matter how the information is stored?arrow_forwardHow does the karyotype of a male differ from the karyotype of a female? Female: Male:arrow_forward
- How might people who have a genetic risk of certain diseases but who show no symptoms exist in a space between the healthy and the sick?arrow_forwardWhy do polygenic characteristics have many phenotypes?arrow_forwarddescribe why some genetic disorders might be dominant,incompletely dominant, or recessive, and give examplesof each?arrow_forward
- What are polygenic diseases?arrow_forwardHow do you think consanguinity is increasing the risk factors of genetic disorders? Explain with examples (at least two). It won’t be possible to change the tradition all of a sudden. If you are a clinical geneticist, how you will be managing this type of community?arrow_forwardWrite a short explanatory essay on the following statement: “Incases of genetically programmed phenotypic plasticity, naturalselection acts on the norm of reaction. Thus the norm of reactionas a whole—rather than any one phenotype—determines ifselection is positive or negative.”arrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
- Human Anatomy & Physiology (11th Edition)BiologyISBN:9780134580999Author:Elaine N. Marieb, Katja N. HoehnPublisher:PEARSONBiology 2eBiologyISBN:9781947172517Author:Matthew Douglas, Jung Choi, Mary Ann ClarkPublisher:OpenStaxAnatomy & PhysiologyBiologyISBN:9781259398629Author:McKinley, Michael P., O'loughlin, Valerie Dean, Bidle, Theresa StouterPublisher:Mcgraw Hill Education,
- Molecular Biology of the Cell (Sixth Edition)BiologyISBN:9780815344322Author:Bruce Alberts, Alexander D. Johnson, Julian Lewis, David Morgan, Martin Raff, Keith Roberts, Peter WalterPublisher:W. W. Norton & CompanyLaboratory Manual For Human Anatomy & PhysiologyBiologyISBN:9781260159363Author:Martin, Terry R., Prentice-craver, CynthiaPublisher:McGraw-Hill Publishing Co.Inquiry Into Life (16th Edition)BiologyISBN:9781260231700Author:Sylvia S. Mader, Michael WindelspechtPublisher:McGraw Hill Education
Human Anatomy & Physiology (11th Edition)
Biology
ISBN:9780134580999
Author:Elaine N. Marieb, Katja N. Hoehn
Publisher:PEARSON
Biology 2e
Biology
ISBN:9781947172517
Author:Matthew Douglas, Jung Choi, Mary Ann Clark
Publisher:OpenStax
Anatomy & Physiology
Biology
ISBN:9781259398629
Author:McKinley, Michael P., O'loughlin, Valerie Dean, Bidle, Theresa Stouter
Publisher:Mcgraw Hill Education,
Molecular Biology of the Cell (Sixth Edition)
Biology
ISBN:9780815344322
Author:Bruce Alberts, Alexander D. Johnson, Julian Lewis, David Morgan, Martin Raff, Keith Roberts, Peter Walter
Publisher:W. W. Norton & Company
Laboratory Manual For Human Anatomy & Physiology
Biology
ISBN:9781260159363
Author:Martin, Terry R., Prentice-craver, Cynthia
Publisher:McGraw-Hill Publishing Co.
Inquiry Into Life (16th Edition)
Biology
ISBN:9781260231700
Author:Sylvia S. Mader, Michael Windelspecht
Publisher:McGraw Hill Education
Genetic Variation and Mutation | 9-1 GCSE Science Biology | OCR, AQA, Edexcel; Author: SnapRevise;https://www.youtube.com/watch?v=bLP8udGGfHU;License: Standard YouTube License, CC-BY