3. Hemophilia is a recessive sex-linked disease carried on the X chromosome in humans. Cross a woman carrier for Hemophilia to a hemophiliac man. Show your solution using Punnett Square. _a.) What % of the offspring will be carrier females? b.) What % will be normal males? c.) What % will be normal females (those who do not have the disease)? _d.) What % will be hemophiliac females? e.) What is the genotype of the carrier female?

3. Hemophilia is a recessive sex-linked disease carried on the X chromosome in humans. Cross a woman carrier for Hemophilia to a hemophiliac man. Show your solution using Punnett Square. _a.) What % of the offspring will be carrier females? b.) What % will be normal males? c.) What % will be normal females (those who do not have the disease)? _d.) What % will be hemophiliac females? e.) What is the genotype of the carrier female?

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Description: 3. Hemophilia is a recessive sex-linked disease carried on the X chromosome in humans. Cross a womancarrier for Hemophilia to a hemophiliac man.Show your solution using Punnett Square.a.) What % of the offspring will be carrier females?b.) What % wi

Biology: The Dynamic Science (MindTap Course List)

4th Edition

ISBN:9781305389892

Author:Peter J. Russell, Paul E. Hertz, Beverly McMillan

Publisher:Peter J. Russell, Paul E. Hertz, Beverly McMillan

Chapter17: Bacterial And Viral Genetics

Section: Chapter Questions

Problem 10TYK

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3. Hemophilia is a sex linked trait that does not allow for blood clotting normally. It is a recessive genetic defect. In the royal family, the mother of the Prince is a carrier for hemophilia. (XHXh) while the father is normal. ( XHY) . What is the genotype of the Prince if he carries the bleeder’s disease? What is the probability that all the female princesses are normal? Use the Punnett square to show your solution.
1. A mother with blood type A has a child with blood type O, and she claims that Mister X is the father. Mister X denies that he could possibly be the father, because he has blood type B. If you were the judge presiding over this case, which of the following arguments would you find most convincing? a. Mr. X could be the father if his blood genotype is IBIB, and the mother’s blood genotype is IAIA b. Mr. X cannot be the father because a child with blood type O cannot have a parent with blood type B c. Mr. X could be the father if his blood genotype is IBi, and the mother’s blood genotype is IAi d. Mr. X cannot be the father because a parent with blood type B cannot have a child with blood type O e. Mr. X cannot be the father because the human ABO blood types are sex-linked traits 2. A monohybrid cross between two pea plants producing yellow peas, resulting in an F1 phenotypic ratio of 3:1 (three yellow pea plants to one green pea plant) indicates what about the parental pea plants?…
4. Define the following terms: A. genotype B. phenotype C. monohybrid D. dihybrid
Assuming no gene linkage, in a dihybrid cross of AABB x aabb with AaBb F1 heterozygotes, what is the ratio of the F1 gametes (AB, aB, Ab, ab) that will give rise to the F2 offspring? a. 1:1:1:1 b. 1:3:3:1 c. 1:2:2:1 d. 4:3:3:1
1. Given the karyotype shown here, is this a male or a female? What would the genotype/phenotype of this individual be?
4. Marfan syndrome is a genetic trait caused by in a dominant allele. The trait causes a weakening of the aorta that can be fatal. A teenager whose mother has the syndrome (but whose maternal grandfather was not affected), and whose father was unaffected, is concerend that she may have the trait. a. What is the phenotype of each of her parents? Genotype? b. What is the chance that the teenager has Marfan syndrome?
2. The common grandfather of two first cousins has hereditary hemochromatosis, a recessive condition causing an abnormal buildup of iron in the body. Neither ofthe cousins has the disease nor do any of their relatives.a. If the first cousins had a child, what is the chancethat the child would have hemochromatosis?Assume that the unrelated, unaffected parents ofthe cousins are not carriers.b. How would your calculation change if you knewthat 1 out of every 10 unaffected people in the population (including the unrelated parents of thesecousins) was a carrier for hemochromatosis?
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.
1.What would you predict would happen if you added Anti-A serum to this type of blood? 2. What would you predict would happen if you added Anti-B serum to this type of blood?3. Why is the genotype that codes for this blood type considered “codominant”?Please answer all of them now and do it
1. Suppose you identify a new gene in mice. One of its alleles specifies white fur, another specifies brown. You want to see if these alleles are inherited in a Mendelian pattern, or with incomplete dominance. What crosses would give you the answer? Explain. 2. Cystic Fibrosis (CF) is an example of a complex genetic disorder caused by a single mutation. Read section 13.1 Menacing Mucus in your text, and explain the cause and symptoms of CF and justify it as an example of pleiotropy.
1.) If Ethidium bromide was not added to a gel, what would happen? 2. How can you tell if an individual is heterozygous for the D1S80 marker?
2. What is the result of crossing over? A. recombination B. mutation C. linkage D. adaptation