1. Hemophilia is a disease inherited as a X-linked recessive trait while pattern baldness iscontrolled by an autosomal gene that is dominant in males and recessive in females.A hemophilic man who is also homozygous for baldness has children with a womanwho is not hemophilic but a carrier and heterozygous normal-haired. Show theparental genotypes, the Genotypic ratio (GR) of the offspring and their phenotypicratio. Separate the total number of the male offspring from female offspring. Forexample, if there are 8 total number of offspring, count how many are females andhow many are males. So if there are 4 females, then the denominator for thegenotypic ratio and phenotypic ratio for female offspring is 4. You can convert it topercentage if you want. Answer the following:a. Among the female offspring, what is the probability of having hemophilic butnormal haired child?b. Among the male offspring, what is the chance of having a child with normal bloodclotting but bald?

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Description: 1. Hemophilia is a disease inherited as a X-linked recessive trait while pattern baldness iscontrolled by an autosomal gene that is dominant in males and recessive in females.A hemophilic man who is also homozygous for baldness has children with a w

X-linked inheritance means that the gene causing the trait or the disorder is located on the X…

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1. Hemophilia is a disease inherited as a X-linked recessive trait while pattern baldness is controlled by an autosomal gene that is dominant in males and recessive in females. A hemophilic man who is also homozygous for baldness has children with a woman who is not hemophilic but a carrier and heterozygous normal-haired. Show the

1. Hemophilia is a disease inherited as a X-linked recessive trait while pattern baldness is controlled by an autosomal gene that is dominant in males and recessive in females. A hemophilic man who is also homozygous for baldness has children with a woman who is not hemophilic but a carrier and heterozygous normal-haired. Show the

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

Chapter12: Mendel, Genes, And Inheritance

Section: Chapter Questions

Problem 7TYK: In cats, the genotype AA produces tabby fur color; Aa is also a tabby, and aa is black. Another gene...

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In cats, the genotype AA produces tabby fur color; Aa is also a tabby, and aa is black. Another gene at a different locus is epistatic to the gene for fur color. When present in its dominant W form (WW or Ww), this gene blocks the formation of fur color and all the offspring are white; ww individuals develop normal fur color. What fur colors, and in what proportions, would you expect from the cross AaWw Aa Ww?
Examine the following pedigrees. Which is the most likely mode of inheritance of each disorder? (a) autosomal recessive (b) autosomal dominant (c) X-linked recessive (d) a, b, or c (e) a or c 9.
Achondroplasia is a rare dominant autosomal defect resulting in dwarfism. The unaffected brother of an individual with achondroplasia is seeking counsel on the likelihood of his being a carrier of the mutant allele. What is the probability that the unaffected client is carrying the achondroplasia allele?
1. An albino man whose parents are both normal marries a woman one of whose parents is normal and the other albino. She has an albino sister. The couple has a normal son. a. Is albinism a dominant or a recessive trait? Explain your answer. b. Give the genotypes of all the persons involved. c.The couple plans to have more kids. What is the probability of their second child being normal?
7. The ability to roll your tongue (R) is dominant to lack of this ability (r). A. What is the genotype of a man who can roll his tongue if his father couldn’t? B. If a man who is heterozygous for tongue rolling marries a woman who is heterozygous, what would you predict for the genotypes and phenotypes of their children?
Classical hemophilia is a sex-linked disease caused by a recessive gene on the X chromosome. (Hemophilia refers to diseases that cause delays in blood clotting.) If a woman who is acarrierof classical hemophilia has children with a normal male, give the ratios of the possible offspring with respect to classical hemophilia. Be sure to state both the genotypes and the phenotypes of each offspring. For genotypes, use X for a normal X chromosome, Xh for an X chromosome with the hemophilia gene, and Y for a normal Y chromosome. For phenotypes, if the offspring is female, be sure to state if homozygous normal, a carrier, or has the disease. If the offspring is a male, be sure to state if normal or has the disease.
1. An albino man whose parents are both normal marries a woman one whose parents is normal and the other albino. She has an albino sister. The couple has a normal son. a. Is albinism a dominant or a recessive trait? Explain your answer. b.Give genotypes of all the persons involved. c. The couple plans to have more kids. What is the probability of their second child being normal?
Two mothers give birth to sons at the same time at a busy urbanhospital. The son of mother 1 has hemophilia, a disease causedby an X-linked recessive allele. Neither parent has the disease.Mother 2 has a son without hemophilia, despite the fact thatthe father has hemophilia. Several years later, couple 1 suesthe hospital, claiming that these two newborns were swappedin the nursery following their birth. As a genetic counselor, youare called to testify. What information can you provide the juryconcerning the allegation?
4. Mr. Salazar has Type A blood while Mrs. Salazar has Type B. They have four children. Bobbie has Type A, Gabbie has Type B, Alex has Type AB, and Teddie has Type O. What are the genotypes of all six people in this family? NOTE: The ABO blood type gene has three alleles. IA and IB are codominant; i (for Type O) is recessive to both.
Hemophilia is an X-linked recessive disease. A hemophilic man marries a woman who is not a carrier of the disease. (a) Draw a Punnett square showing the genotypes of their children. (b) What are the chances that their daughters will be carriers of the disease? (c) What percentage of their children are likely to have the disease?
1. Use the diagram of the pedigree above, which shows inheritance of an x-linked recessive trait through a family. Select ALL of the individuals in the pedigree who must be carriers for the trait. E G B C H A
.Hemophilia is a blood-clotting disorder in humans that followsan X-linked recessive pattern of inheritance. A man with hemophilia and a woman without hemophilia have a daughter withhemophilia. If you let H represent the normal allele and h thehemophilia allele, what are the genotypes of the parents?a. Mother is XHXhand father is XhY.b. Mother is XhXhand father is XhY.c. Mother is XhXhand father is XHY.d. Mother is XHXhand father is XHY