EP CONNECT ONLINE ACCESS FOR BIOLOGY:
5th Edition
ISBN: 9781260542226
Author: Hoefnagels
Publisher: MCGRAW-HILL HIGHER EDUCATION
expand_more
expand_more
format_list_bulleted
Concept explainers
Videos
Textbook Question
Chapter 35, Problem 8MCQ
A chemical that can cause a birth defect is a
a. toxin.
b. trisomy.
c. mutagen.
d. teratogen.
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solution
Students have asked these similar questions
A female born with Angelman syndrome carries a deletion in theAS gene (i.e., the UBE3A gene). Which parent transmitted thedeletion to her?a. Her father c. Either her mother or fatherb. Her mother
If a genetic disease is inherited on the basis of an autosomal dominant gene, one would expect
to find which of the following?
A. Affected fathers have only affected children.
B. Affected mothers never have affected sons.
C. If both parents are affected, all of their offspring have the disease.
D. If a child has the disease, one of his or her grandparents also had the disease.
Select the letter of the choice that best completes the statement. An extra chromosome can cause a defect known as trisomy 21 ora. Cooley’s anemia.b. Huntington’s disease.c. Down syndrome.d. PKU.
Chapter 35 Solutions
EP CONNECT ONLINE ACCESS FOR BIOLOGY:
Ch. 35.1 - Prob. 1MCCh. 35.1 - Prob. 2MCCh. 35.1 - Prob. 3MCCh. 35.2 - Prob. 1MCCh. 35.2 - Prob. 2MCCh. 35.2 - Prob. 3MCCh. 35.2 - Prob. 4MCCh. 35.3 - Prob. 1MCCh. 35.3 - Prob. 2MCCh. 35.3 - How do hormones regulate the ovarian and menstrual...
Ch. 35.4 - Prob. 1MCCh. 35.4 - Prob. 2MCCh. 35.4 - Prob. 3MCCh. 35.5 - What are the events of fertilization?Ch. 35.5 - What are the relationships among the zygote,...Ch. 35.5 - What is implantation, and when does it occur?Ch. 35.5 - Prob. 4MCCh. 35.5 - Prob. 5MCCh. 35.5 - What are the events of the second and third...Ch. 35.5 - Prob. 7MCCh. 35.6 - Prob. 1MCCh. 35.6 - Prob. 2MCCh. 35.6 - Prob. 3MCCh. 35.7 - Prob. 1MCCh. 35.7 - Prob. 2MCCh. 35 - Prob. 1MCQCh. 35 - Which hormones play central roles in both male and...Ch. 35 - Prob. 3MCQCh. 35 - Why can't a fertilized polar body develop into a...Ch. 35 - Prob. 5MCQCh. 35 - Prob. 6MCQCh. 35 - What is the correct order of structures to develop...Ch. 35 - A chemical that can cause a birth defect is a a....Ch. 35 - Prob. 1WIOCh. 35 - Prob. 2WIOCh. 35 - Prob. 3WIOCh. 35 - Prob. 4WIOCh. 35 - Prob. 5WIOCh. 35 - Prob. 6WIOCh. 35 - Is each of the following cell types haploid or...Ch. 35 - Prob. 8WIOCh. 35 - Prob. 9WIOCh. 35 - What would happen if two sperm fertilized the same...Ch. 35 - Prob. 11WIOCh. 35 - Prob. 12WIOCh. 35 - Prob. 13WIOCh. 35 - Prob. 14WIOCh. 35 - Prob. 15WIOCh. 35 - Prob. 16WIOCh. 35 - Prob. 17WIOCh. 35 - Prob. 18WIOCh. 35 - Prob. 19WIOCh. 35 - Review the Survey the Landscape figure in the...Ch. 35 - Add ovulation to the concept map. What hormonal...Ch. 35 - Add the terms placenta, follicle, polar body,...
Additional Science Textbook Solutions
Find more solutions based on key concepts
Describe Mendels conclusions about how traits are passed from generation to generation.
Concepts of Genetics (11th Edition)
Match the people in column A to their contribution toward the advancement of microbiology, in column B. Column ...
Microbiology: An Introduction
How does the removal of hydrogen atoms from nutrient molecules result in a loss of energy from the nutrient mol...
Seeley's Anatomy & Physiology
1. Genetics affects many aspects of our lives. Identify three ways genetics affects your life or the life of a ...
Genetic Analysis: An Integrated Approach (3rd Edition)
Why is it necessary to be in a pressurized cabin when flying at 30,000 feet?
Anatomy & Physiology (6th Edition)
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
- In humans, hemophilia is an X-linked recessive condition characterized by the inability of blood to clot normally. A woman who is a carrier for hemophilia marries a man who has hemophilia. What are the genotypes of the woman and man, respectively? a. xH+xH+, xH+y b. xH+xH xH+y c. xH+xH xHy Od. XHXH, XH+y O e. xHxH xHyarrow_forwardMales can be said to be ‘weaker’ genetically because they are predisposed to disorders that are a result of sexually linked transmission. This is mainly because their genotype for ‘male’ is “spelled” as: A. XX B. DNA C. XY D. BBarrow_forwardJoe has classic hemophilia, an X-linked recessive disease. Could Joe have inherited the gene for this disease from the following people? Yes No a. His mother's mother b. His mother's father c. His father's mother d. His father's fatherarrow_forward
- von Gierke's disease is inherited as A. Autosomal dominant B. Autosomal recessive C. X-linked recessive D. X-linked dominantarrow_forwardIn order for a male to inherit a sex-linked (X-linked) disorder, he must receive the allele from: a. his mother only. b. either his mother or father. c. his father only. d. both his mother and father.arrow_forwardOne of the forms of rickets is inherited in the autosomal dominant way. This disease is a result of: Select one: a. Aneuploidy. O b. Changes in the number of chromosomes. c. Chromosomal mutations. e. Gene mutations. O d. Polyploidy.arrow_forward
- Hemophilia in humans is due to a mutation on the X chromosome. What will be the result of mating between a normal (non-carrier) female and a hemophiliac male? A. Half of the daughters are normal and half of the sons are hemophiliacs. B. All sons are normal and all daughters are carriers. C. All daughters are normal and all sons are carriers. D. Half of the children are normal and the other half are hemophiliacs; All daughters are carriers.arrow_forward------ is the transmission of DNA to offspring. a. Reproduction b.Development c. Homeostasis d. Inheritancearrow_forwardAn individual who is a carrier for a sex-linked trait such as hemophilia Select one: A. is always female. B. is homozygous for the recessive condition. C. cannot pass the gene on to his or her daughters. D. shows the dominant phenotype.arrow_forward
- A young man went to the doctor because he had small testes and enlarged breasts. Through chromosomal testing, it was determined that this young man had the sex chromosomes XXY. Identify the syndrome with which this young man was MOST likely diagnosed. A. Turner syndrome B. Klinefelter syndrome C. Cri du Chat syndrome D. Down syndromearrow_forwardHemophilia is a disease caused by a gene found on the X chromosome. Therefore, it is a sex-linked disease which is caused by the recessive allele. Suppose, a man with hemophilia marries a woman who is homozygous dominant for the trait. Predict the genotype of the man. (XH = normal; Xh= hemophiliac) * a. XH Y b. XHXh c. XhXh d. Xh Yarrow_forwardA 14-year-old girl has some abnormalities: her height is lower than that of the girls of the same age, the signs of puberty are absent, her neck is very short, her shoulders are wide. During the cytogenetic analysis the lack of one X-chromosome was found. The girl has normal intellectual development. What disease does the girl have? Select one: a. Turner's syndrome. b. Down's syndrome. c. Edward's syndrome. d. Patau syndrome. O e. Klinefelter's syndrome.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:PEARSON
Biology 2eBiologyISBN:9781947172517Author:Matthew Douglas, Jung Choi, Mary Ann ClarkPublisher:OpenStax
Anatomy & 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 & Company
Laboratory 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
Mitochondrial mutations; Author: Useful Genetics;https://www.youtube.com/watch?v=GvgXe-3RJeU;License: CC-BY