Gen Combo Ll Biology; Connect W/learnsmart Labs Access Card
4th Edition
ISBN: 9781259853197
Author: Robert Brooker
Publisher: MCGRAW-HILL HIGHER EDUCATION
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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
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For each of the following chromosome complements, what is the phenotypic sex of a person who has a. XY with the SRY gene deleted? b. XX with a copy of the SRY gene on an autosomal chromosome? c. XO with a copy of the SRY gene on an autosomal chromosome? d. XXY with the SRY gene deleted? e. XXYY with one copy of the SRY gene deleted?
ch of the following best describes why males cannot be carriers of sex-linked traits?
A. Males cannot be carriers because their Y chromosome makes them immune to sex-linked traits
B. This is incorrect, males can be carriers of sex-linked traits
O C. Males cannot be carriers because they only inherit one X chromosome, either having the trait or not
O D. Males cannot be carriers because their mothers pass on an X chromosome without the sex-linked trait
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.
Chapter 16 Solutions
Gen Combo Ll Biology; Connect W/learnsmart Labs Access Card
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...
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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_forwardFragile 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_forward
- Which 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_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_forwardA 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_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_forwardExplain why a person with Klinefelter Syndrome (XXY) still exhibits abnormal phenotypes despite the fact that one of the extra X Chromosome is inactivated practically leaving an XY active sex chromosomes similar to a normal male?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
- 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_forwardWhat is the phenotype of a person who has XXXY sex chromosomes? a. Klinefelter syndromeb. Turner syndromec. Poly-X femalearrow_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
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