Biology (MindTap Course List)
11th Edition
ISBN: 9781337392938
Author: Eldra Solomon, Charles Martin, Diana W. Martin, Linda R. Berg
Publisher: Cengage Learning
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Chapter 11.3, Problem 8LO
Discuss the genetic determination of sex and the inheritance of X-linked genes in mammals.
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Explain the difference between X-linked recessive traits and X-linked dominant traits. What are the possibilities that a female child will be affected and express each of the traits?
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Chapter 11 Solutions
Biology (MindTap Course List)
Ch. 11.1 - Define the terms phenotype, genotype, locus,...Ch. 11.1 - Describe Mendels principles of segregation and...Ch. 11.1 - Distinguish among monohybrid, dihybrid, and test...Ch. 11.1 - Explain Mendels principles of segregation and...Ch. 11.1 - What is the maximum number of different alleles...Ch. 11.1 - Can Mendels principle of segregation be...Ch. 11.1 - Prob. 3CCh. 11.2 - PREDICT Use the rules of probability to answer the...Ch. 11.2 - In answering the previous question, did you use...Ch. 11.3 - Define linkage and relate it to specific events in...
Ch. 11.3 - Show how data from a two-point test cross can be...Ch. 11.3 - Discuss the genetic determination of sex and the...Ch. 11.3 - What ratio of genotypes to phenotypes is observed...Ch. 11.3 - Prob. 2CCh. 11.3 - CONNECT Two loci exhibit 5% recombination between...Ch. 11.3 - Which chromosome determines the male sex in humans...Ch. 11.3 - Prob. 5CCh. 11.4 - Explain some of the ways genes may interact to...Ch. 11.4 - Distinguish among incomplete dominance,...Ch. 11.4 - Prob. 11LOCh. 11.4 - Prob. 1CCh. 11.4 - What is the difference between multiple alleles...Ch. 11.4 - Prob. 3CCh. 11.4 - Prob. 4CCh. 11 - One of the autosomal loci controlling eye color in...Ch. 11 - The F1 flies described in question 1 were mated...Ch. 11 - The type of cross described in question 2 is (a)...Ch. 11 - Individuals of genotype AaBb were crossed with...Ch. 11 - Assume that the ratio of females to males is 1:1....Ch. 11 - Redgreen color blindness is an X-linked recessive...Ch. 11 - When two long-winged flies were mated, the...Ch. 11 - The long hair of Persian cats is recessive to the...Ch. 11 - Mr. and Mrs. Smith are concerned because their own...Ch. 11 - A walnut comb rooster is mated to three hens. Hen...Ch. 11 - Individuals of genotype AaBb were mated to...Ch. 11 - Genes A and B are 6 map units apart, and A and C...Ch. 11 - VISUALIZE Sketch a series of diagrams showing each...Ch. 11 - Can you always ascertain an organisms genotype for...Ch. 11 - CONNECT Compare the mechanisms of genetic...Ch. 11 - EVOLUTION LINK Darwins theory of evolution by...Ch. 11 - INTERPRET DATA Using the graph in Figure 11-20,...
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- The gene causing Coffin-Lowry syndrome (OMIM 303600) was recently identified and mapped on the human X chromosome. Coffin-Lowry syndrome is a rare disorder affecting brain morphology and development. It also produces skeletal and growth abnormalities, as well as abnormalities of motor control. Coffin-Lowry syndrome affects males who inherit a mutation of the X-linked gene. Most carrier females show no symptoms of the disease but a few carriers do. These carrier females are always less severely affected than males. Offer an explanation for this finding.arrow_forward. In humans, hemophilia is an X-linked recessive gene and will only be expressed in females if they are homozygous for this gene. However, in some rare cases, a heterozygote becomes hemophilic. Explain how this incident happens and why will there be skewed X-inactivation?arrow_forwardDescribe how X-linked traits are inherited and explain how X-linked inheritance is different from simple dominance inheritancearrow_forward
- Could a woman who expresses the x-linked color-blind trait have a son with normal vision?arrow_forwardWhat characteristics are exhibited by an X-linked trait?arrow_forwardWhich findings support the fact that the presence of the Y- chromosome rather than the lack of a second X-chromosome determines the development of maleness in mammals? A transgenic mouse with two X-chromosomes and the SRY gene from the Y-chromosome develops male sex organs. A human with an XXXY genotype (Klinefelter syndrome) is phenotypically male. A human with an XO genotype (Turner syndrome) is phenotypically female. a and b, but not c a, b, and carrow_forward
- Males of many diploid species (like us) have X and Y sex chromosomes. They are hemizygous for most X- linked genes. Thus, males express most X-linked alleles, whether they are dominant or recessive in females. In the fruit fly Drosophila, it is common to achieve the equivalent of a test cross of X-linked genes in females by assessing the readily observed phenotypes of their male progeny. Since males do not receive X-linked genes from their father, sires of these crosses can be normal or wild-type flies. In fly genetics, it is conventional to name a gene after the mutant phenotype that enabled its discovery. Your challenge is to establish gene order and map distances between three X-linked genes in Drosophila. Each gene is represented by recessive mutant alleles that express rather distinctive phenotypes relative to their dominant wild-type alternative alleles. Flies expressing fruitless (f) are bisexual, lush (1) have a heightened responses to ethanol, and ken&barbie (kb) lack external…arrow_forwardWhat is x linked genes?arrow_forwardLauren reports that she had a maternal male cousin (through a maternal aunt) and a maternal great uncle (maternal grandmother’s brother) both pass away from the same x-linked lethal condition. Both affected individuals did not have genetic testing. Lauren has a normal carrier screen for x-linked lethal conditions, which you know identifies 40% of causative mutations. If Lauren is currently pregnant with a male child, what is the chance that this child will have the condition?arrow_forward
- How is the inheritance of X-linked traits different from the inheritance of autosomal traits? How is the inheritance of X-linked and Autosomal traits similar? Please make a list of all similarities and differences. Please list a many differences and similarities as possible.arrow_forwardNote: Don't copy from internet, Also answer correctly in terms of diploid, hemizygous, and carrier!! Thanks Explain why genetic disorders caused by recessive alleles of X-linked genes appear more frequently in males than in females? In your explanation, please include explanations of the following terms: diploid, hemizygous, carrier.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_forward
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