EBK BIOLOGY
4th Edition
ISBN: 8220102797376
Author: BROOKER
Publisher: YUZU
expand_more
expand_more
format_list_bulleted
Concept explainers
Videos
Textbook Question
Chapter 16, Problem 9TY
Genes located on a sex chromosome are said to be
- a. X-linked.
- b. dominant.
- c. hemizygous.
- d. sex-linked.
- e. autosomal
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 is not a characteristic of X-linked recessive traits in humans?
a.
Approximately one-half of the sons of a female carrier are affected.
b.
More males than females affected.
c.
Phenotypically normal daughters of affected men are always carriers.
d.
They cannot be passed from father to son.
e.
Affected daughters always have an affected mother.
In 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.
During the observation of a baby the diagnosis of Down's syndrome was made. What is the main cause of this pathology?
Select one:
a. Trisomy on the 13-th chromosome.
b. Trisomy on the 21-st chromosome.
c. Trisomy on X chromosome.
d. Monosomy on the 1-st chromosome.
O e. Undivergence of sex chromosomes.
Chapter 16 Solutions
EBK BIOLOGY
Ch. 16.1 - Prob. 1CCCh. 16.1 - Prob. 2CCCh. 16.1 - Prob. 3CCCh. 16.1 - Prob. 4CCCh. 16.1 - Prob. 5CCCh. 16.1 - Mendels Laws of Inheritance Concept Check: What...Ch. 16.2 - Prob. 1BCCh. 16.2 - Prob. 2BCCh. 16.2 - Prob. 1CCCh. 16.3 - Prob. 1CC
Ch. 16.3 - Prob. 2CCCh. 16.4 - Prob. 1CCCh. 16.4 - Prob. 1EQCh. 16.4 - Prob. 2EQCh. 16.4 - Prob. 3EQCh. 16.5 - Prob. 1CCCh. 16 - Prob. 1TYCh. 16 - During which phase of nuclear division does the...Ch. 16 - Prob. 3TYCh. 16 - Which of Mendels laws cannot be observed in a...Ch. 16 - During a __________blank, an individual with the...Ch. 16 - Prob. 6TYCh. 16 - Prob. 7TYCh. 16 - A hypothetical flowering plant species produces...Ch. 16 - Genes located on a sex chromosome are said to be...Ch. 16 - Prob. 10TYCh. 16 - Prob. 1CQCh. 16 - A cross is made between individuals having the...Ch. 16 - Core Concept: Systems We can view life as a...Ch. 16 - Discuss the principles of the chromosome theory of...Ch. 16 - When examining a human pedigree, what patterns do...
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
- Fragile X syndrome is an X-linked recessive Achondroplasia is an autosomal dominant trait characterized by a shortened stature. An XX individual is a carrier for Fragile X disorder and is unaffected by achondroplasia. An XY individual is not affected by Fragile X disorder and has achondroplasia. a. What is the XX individual’s genotype b. What is the XY individual’s genotype? c. If the two individuals where to have children, what are the possible genotypes and phenotypes of their children? Use a Punnett square. d. What is the probability of them having a child with Fragile X and achondroplasia?arrow_forwardFragile X is a disorder which causes mental impairment in affected individuals. The trait which is due to a mutation in the FMR1 gene on the X chromosome is inherited in a recessive manner. An unaffected son was born to an affected man and an unaffected woman. The woman’s mother was affected while the father was normal. a. Indicate the gene notation. b. Give the genotype of the son. c. Is it possible for the couple to have an affected daughter? affected son? Derive the genotypic and phenotypic ratios for the offspring. Show and label your solutions properly. d. If the couple has four children, what is the probability that they will have three normal daughters and one normal son?arrow_forwardWhich of the below explains why trisomy is better tolerated in humans than monosomy? (Select all correct options). a. Loss of heterozygosity in monosomy b. Increased gene expression in trisomic cells is beneficial c. Reduced gene expression in monosomy d.The extra chromosome in trisomic cells is degraded Which two are both necessary to hold a tetrad together until Anaphase I? a) nondisjunction b) cross over c) centromere cohesion d) synaptonemal complex e) separese activityarrow_forward
- A male has a particular X-linked recessive genetic disorder. His partner is normal, but her father had the disorder. What is the chance that their sons will have the disorder? Select one: Oa. 50% O b. 0% O c. 100% O d. impossible to determine from the information given. O e. 25% LENA C Transcribed Image Text: A male has a particular X-linked recessive genetic disorder. His partner is normal, but her father had the disorder. What is the chance that their sons will have the disorder? Select one: O a. 50% O b. 0% O c. 100% O d. impossible to determine from the information given. O e. 25% Po 11 W *****arrow_forwardConsider a couple: a woman who is homozygous for a recessive mutation that causes X-linked colorblindness, and a man with full color vision (he does not carry a copy of the mutation). a) What is the probability that a son of this couple will be colorblind? b) What is the probability that a daughter of the couple will be colorblind?arrow_forwardColor blindness in humans is an X-linked recessive trait. This means that... O a. Females are more likely to be color blind than males b. The gene associated with color blindness is found on the X chromosome, and an individual must have one (in males) or two (in females) mutant copies of the allele in order to be diagnosed as being color blindarrow_forward
- Which of the following statements is FALSE? Inactivation of one of the two X chromosomes in the somatic cells of mammalian females..... a. underlies the Calico phenotype in cats. b. leads to cellular mosaicism in females heterozygous for an X-linked gene. c. affects 75 % of the paternal and 25 % of the maternal X-chromosomes of a mammalian body. d. leads to the formation of a Barr body in female cells' nuclei. e. is the mechanism in mammals to compensate for the higher dosage of X-linked genes in females as compared to males.arrow_forwardIn a karyotype of a man whose wife has had several miscarriages, it was discovered that he had onlv 45 chromosomes. However, he displayed no obvious phenotypic defects. Furthermore, one of the chromosomes of pair 15 was abnormally long. Which of the following terms best describes the condition of this man? a. monosomy b,. trisomy c. tetrasomy d. translocation carrier e. edward syndormearrow_forwardWhich of the following disorders in humans has an X-linked recessive inheritance pattern? a.Hutchinson-Gilford progeria b.Tay-Sachs disease c.Marfan syndrome d.Red-green color blindness Which of the following is described as a structural rearrangement of a chromosome in which a broken piece has become reattached in the wrong location? a.Duplication b.Translocation c.Inversion d.Deletion Which of the following disorders arises from translocation events? a.Huntington’s disease b.Infertility c.Burkitt lymphoma d.Duchenne muscular dystrophyarrow_forward
- Choose correct option and do explain. Considering an X-linked dominant trait, if an affected woman and an unaffected man decide to have children, which of the answer choices is possible for their children? a. All of their sons are expected to show the dominant trait. b. Their daughters are expected be heterozygous for the gene. c. Their daughters are not expected to show the dominant trait. d. Their sons are expected to be heterozygous for the gene. e. All their children, whether male or female, are expected to show the dominant trait.arrow_forwardA patient has mental deficiency, a short stature, and the mongolian type of the eyelid fold. The microscopical examination of the patient's karyotype revealed the presence of trisomy on the 21-st chromosome. What do we call the disease which is caused by this chromosomal abnormality? Select one: a. Down's syndrome. b. Klinefelter's syndrome. O c. Turner's syndrome. d. Edward's syndrome. e. Patau syndrome.arrow_forwardWhich of the following statements is TRUE? Overexpression of the X-chromosome in the somatic cells of males a. leads to the formation of a Barr body in male cells' nuclei. b. leads to cellular mosaicism in males hemizygous for an X-linked gene. c. is characteristic of all XY systems of sex determination. d. is the mechanism in flies to compensate for the higher dosage of X-linked genes in females as compared to males. e. None of the abovearrow_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
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