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Genetics: From Genes to Genomes, 5th edition
5th Edition
ISBN: 9780073525310
Author: Leland H. Hartwell, Michael L. Goldberg, Janice A. Fischer, Leroy Hood, Charles F. Aquadro
Publisher: McGraw-Hill Education
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Textbook Question
Chapter 3, Problem 9P
Assuming no involvement of the Bombay phenotype:
a. | If a girl has blood type O, what could be the genotypes and corresponding |
b. | If a girl has blood type B and her mother has blood type A, what genotype(s) and corresponding phenotype(s) could the other parent have? |
c. | If a girl has blood type AB and her mother is also AB, what are the genotype(s) and corresponding phenotype(s) of any male who could not be the girl’s father? |
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Blood types in humans are Codominant.
a. What are the possible genotypes of someone with type O blood?
b. What are the possible genotypes of someone with type B blood?
c. What is the phenotype of someone’s whose genotype is AO?
d. A man with AB blood is married to a woman with AB blood. What blood types will their children be and in what proportion?
Suppose a woman has four sons, and two are colorblind but have normal blood clotting and two have hemophilia but normal color vision. What is the probable genotype of the woman?
b. Suppose this woman (later on) had a son with normal vision and normal blood clotting. How can this be explained?
Duchenne muscular dystrophy is sex linked and usually affects only males. Victims of the disease become progressively weaker, starting early in life.a. What is the probability that a woman whose brother has Duchenne’s disease will have an affected child?b. If your mother’s brother (your uncle) had Duchenne’s disease, what is the probability that you have received the allele?c. If your father’s brother had the disease, what is the probability that you have received the allele?
Chapter 3 Solutions
Genetics: From Genes to Genomes, 5th edition
Ch. 3 - For each of the terms in the left column, choose...Ch. 3 - In four-oclocks, the allele for red flowers is...Ch. 3 - The Aa heterozygous snapdragons in Fig. 3.3 are...Ch. 3 - In the fruit fly Drosophila melanogaster, very...Ch. 3 - A cross between two plants that both have yellow...Ch. 3 - In radishes, color and shape are each controlled...Ch. 3 - A wild legume with white flowers and long pods is...Ch. 3 - Prob. 8PCh. 3 - Assuming no involvement of the Bombay phenotype:...Ch. 3 - Several genes in humans in addition to the ABO...
Ch. 3 - Alleles of the gene that determines seed coat...Ch. 3 - Prob. 12PCh. 3 - In a population of rabbits, you find three...Ch. 3 - In clover plants, the pattern on the leaves is...Ch. 3 - Fruit flies with one allele for curly wings Cy and...Ch. 3 - Prob. 16PCh. 3 - In a species of tropical fish, a colorful orange...Ch. 3 - A rooster with a particular comb morphology called...Ch. 3 - A black mare was crossed to a chestnut stallion...Ch. 3 - Prob. 20PCh. 3 - Prob. 21PCh. 3 - a. How could you describe inheritance of flower...Ch. 3 - Explain the difference between epistasis and...Ch. 3 - The dominant allele H reduces the number of body...Ch. 3 - Secretors genotypes SS and Ss secrete their A and...Ch. 3 - Normally, wild violets have yellow petals with...Ch. 3 - Prob. 27PCh. 3 - Three different pure-breeding strains of corn that...Ch. 3 - In mice, the AY allele of the agouti gene is a...Ch. 3 - A student whose hobby was fishing pulled a very...Ch. 3 - Prob. 31PCh. 3 - Prob. 32PCh. 3 - Three genes in fruit flies affect a particular...Ch. 3 - The garden flower Salpiglossis sinuata painted...Ch. 3 - In foxgloves, there are three different petal...Ch. 3 - In a culture of fruit flies, matings between any...Ch. 3 - Suppose that blue flower color in a plant species...Ch. 3 - Prob. 38PCh. 3 - Considering your answers to Problem 38, does the...Ch. 3 - Prob. 40PCh. 3 - Prob. 41PCh. 3 - Familial hypercholesterolemia FH is an inherited...Ch. 3 - You have come into contact with two unrelated...Ch. 3 - Polycystic kidney disease is a dominant trait that...Ch. 3 - Using each of the seven coat color genes discussed...
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- A man who has color blindness and type O blood has children with a woman who has normal color vision and type AB blood. The woman’s father had color blindness. Color blindness is determined by an X-linked gene, and blood type is determined by an autosomal gene. a. What are the genotypes of the man and the woman? b. What proportion of their children will have color blindness and type B blood? c. What proportion of their children will have color blindness and type A blood? d. What proportion of their children will be color blind and have type AB blood?arrow_forward15. The following pedigree shows inheritance of Huntington's disease, a fatal genetic disorder that causes neurodegeneration. Since signs and symptoms usually do not appear until adulthood, many who are carriers may not realize their risk of passing on the disease-causing allele. The following pedigree represents a family in which some people are affected by Huntington's disease. Reeessive Trit er btmnt be Mec yplicalty Hinheteearrow_forwardA man with type B blood marries a woman with type A blood. They have the first child with blood type O. a. What are the genotypes of the father and the mother? b. What is the genotype and phenotype of the baby?arrow_forward
- Assume that one of Merida's sons, who is heterozygous for orange hair color, married a girl that was also heterozygous. Create a Punnett square to show the possibilities that would result if they had children. a. List the possible genotypes and phenotypes for their children. b. What are the chances of a child with orange hair? c. What are the chantes of a child with yellow?arrow_forwardIn humans, having freckled skin (F) is dominant. Assume that a homozygous recessive man and a heterozygous woman have a child. a. What is the woman's phenotype? b. Show the Punnett square for the cross. С. What is the child's probability of having no freckles? Uuntarrow_forwardSickle cell anemia is an inherited red blood cell disorder in which there are not enough healthy red blood cells to carry oxygen throughout the body. The allele that causes sickle-cell anemia is autosomal recessive (s), and the dominant allele can be represented by S. How many offspring will be affected by the disorder if the mother is a carrier, and the father appears to be normal? (Include the gender) a. b. How many will become carriers? (include the gender) A- 三三三 四 四 II !!arrow_forward
- Curly hair (C) is dominant to straight hair (c). Is it possible for a curly haired man to produce curly haired children if his wife has straight hair? Explain your answer based on a Punnett square.arrow_forwardc) What blood types could be observed in children born to a woman who has blood type A and a man who has blood type AB? Draw a Punnett square to prove your answers.arrow_forwardA woman who has A blood type (her mother had blood type A and her father had blood type B- a child with a man with blood type AB (his mother was blood type A and his father was blood t AB) Answer the following questions. [ Select ] Ai 1. What is the genotype of the woman's father v Bi ii BB 2. What is the genotype of the woman? AB AB not enough information to determine 3. What is the genotype of the man's mother? Ai 4. What is the possibility of the man and woman having a child with blood type O? 50% 5. What is the possibility of the man and woman having a child with blood type A? [ Select ] 6. Is it possible for the woman to have a brother with blood type O? Yes Alleles: Ig =B lA =A 80 888 F8 F9 F7 F5 F6 F2 F3 F4 & 23 24 5arrow_forward
- Hemophilia is a disease caused by a gene found on the X chromosome. Therefore, it is referred to as a sex-linked disease. The recessive allele causes the disease. A man with hemophilia (xhy) marries a woman who is homozygous dominant (XHXH. A. Illustrate using a Punnett square the probability that their children will have the disease. B. Will any of their children have the disease? C. Predict the probabilities of their children having the disease.arrow_forwardA woman with a rare autosomal recessive disorder was told that it was unlikely that her children would have the disorderas her husband did not have it. However, her first child has the disorder. a. What is the most likely explanation? b. Diagram the cross between the woman and her husband using a Punnett square, give the genotypic ratio (GR) and phenotypic ratio (PR) from the Punnett square. c. Based on the Punnett square results, what is the chance that her next child will have the disorder?arrow_forwardA couple with the following blood types: the man has type AB and the woman has type B, discover their child has type O blood. Is it possible that one of these ‘parents’ may not actually be the genetic parent of this child? If so, which one, and how do you know?arrow_forward
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