Someone please help with each question, they are all about the same pedigree. The first question the option is (DOMINANT OR RECESSIVE)The bottom part of the second image the cut off part asks:"For the next question, give the probability as a fraction that is simplified to the lowest value. Type your fraction in #/# format without spaces. For example, one-half should be typed as 1/2. Failure to follow these instructions will result in your answer being marked as incorrect. Suppose that III-4 and III-5 were to have a child. What is the probability that their first child will be a daughter that has the disorder? __________"Someone please help with each question on the image and the cut off part that I types above. Refer to the pedigree below for this question. Individuals who are shaded have anX-linked disorder. Those who are not shaded have the normal phenotype. Let "A"and "a" represent the dominant and recessive alleles, respectively.The disorder represented by the shaded symbol isphenotype.to the normalA list of possible genotypes is given below. Determine the appropriate genotypefor each individual. Type in the number for the correct answer in the spaceprovided. Do not type anything else in the space. It is ok to use an answer morethan one time.1. XÂY2. Xa Y3. XA XAAVA6. 1/2 XA XA + 1/2 X X³7. 1/4 X^ X^ + 3/4 X^ X®xảA?8. 3/4 XA XA + 1/4 XA X A list of possible genotypes is given below. Determine the appropriate genotypefor each individual. Type in the number for the correct answer in the spaceprovided. Do not type anything else in the space. It is ok to use an answer morethan one time.1. XÂY2. Xa Y3. XA XA4. XA Xa5. Xa xaThe genotype of individual 1-1 isThe genotype of individual II-2 isThe genotype of individual III-4 isThe genotype of individual III-5 isА6. 1/2 XA XA + 1/2 XA XªSN7. 1/4 X^ X^ + 3/4 X^ XªXA8. 3/4 X X + 1/4 XA X²9. 1/3 X X + 2/3 X X³10. 2/3 XA XA + 1/3 XA X²For the next question, give the probability as a fraction that is simplified to thelowest value. Type your fraction in #/# format without spaces. For example, one-half should be typed as 1/2. Failure to follow these instructions will result in youranswer. being marked as incorrect.A?

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Description: Someone please help with each question, they are all about the same pedigree. The first question the option is (DOMINANT OR RECESSIVE)The bottom part of the second image the cut off part asks:"For the next question, give the probability as a fractio

This is an autosomal dominant X linked disorder meaning that the mutation is present on X…

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Someone please help with each question, they are all about the same pedigree. The first question the option is (DOMINANT OR RECESSIVE) The bottom part of the second image the cut off part asks: "For the next question, give the probability as a fraction that is simplified to the lowest value. Type your fraction in #/# format without spaces. For example, one-half should be typed as 1/2. Failure to follow these instructions will result in your answer being marked as incorrect. Suppose that III-4 and III-5 were to have a child. What is the probability that

Someone please help with each question, they are all about the same pedigree. The first question the option is (DOMINANT OR RECESSIVE) The bottom part of the second image the cut off part asks: "For the next question, give the probability as a fraction that is simplified to the lowest value. Type your fraction in #/# format without spaces. For example, one-half should be typed as 1/2. Failure to follow these instructions will result in your answer being marked as incorrect. Suppose that III-4 and III-5 were to have a child. What is the probability that

Human Heredity: Principles and Issues (MindTap Course List)

11th Edition

ISBN:9781305251052

Author:Michael Cummings

Publisher:Michael Cummings

Chapter6: Cytogenetics: Karyotypes And Chromosome Aberrations

Section: Chapter Questions

Problem 2QP: Given the karyotype shown at right, is this a male or a female? Normal or abnormal? What would the...

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Refer to the pedigree below for this question. Individuals who are shaded have an X-linked disorder. Those wha are not shaded have the normal phenotype. Let "A" and "a" represent the dominant and recessive alleles, respectively. The disorder represented by the shaded symbol to the normal phenotype. Recessive Daminant A list of possible genotypes is given below. Determine the appropriate genotype for each individual. Type in the number for the correct answer in the space provided. Do not type anything else in the space. It is ok to use an answer more than one time. 1. XАY 6. 1/2 x^ x^ + 1/2 x^ x* 7. 1/4 X^ x* + 3/4 x^ x° 8. 3/4 X^ x^ + 1/4 x^ x 9. 1/3 x^ x* + 2/3 X^ x 10. 2/3 х* х* + 1/3 х^ х 2. X Y 3. ХА ХА 4. X^ X 5. X X The genotype of individual -2 is The genotype of individual -3 is The genotype of individual Il-5 is The genotype of individual II-7 is The genotype of individual lll-3 is
Refer to the pedigree below for this question. Individuals who are shaded have an X-inked disorder. Those who are not shaded have the normal phenotype. Let "A" and "a" represent the dominant and recessive alleles, respectively. The disorder represented by the shaded symbol to the normal phenotype. Recessive Dominant A list of possible genotypes is given below. Derermine the appropriate genotype for each individual. Type in the number for the correct answer in the space provided. Do not type arything else in the space. It is ok to use an answer more than one time. 6. 1/2 x^ x^ + 1/2 x^ x 7. 1/4 X x^ +3/4 x^x 8. 3/4 X^ x^ + 1/4 x^ x 9. 1/3 x^ x^ + 2/3 x^ X" 10. 2/3 x^ x^ + 1/3 X^ x* 1. X^ Y 2. X Y 3. X^ xA 4. X^ X 5. X* х The genotype of individual I-1 is The genotype of individual II-5 is The genotype of individual I1-6 is The genotype of individual ill-6 is For the next question, give the probability as a fraction that is simplified to the lowest value. Type your fraction in # format…
A mother is heterozygous for the X-linked gene for colorblindness and also heterozygous for the autosomal inherited sickle cell anemia. She is married to a man who can see color normally and who is heterozygous for sickle cell trait. Using b (colorblind), B (normal color), S (normal hemoglobin), s (sickle cell), answer the following: a. What are the genotypes of the parents? b: What is the probability of having a child who is both color blind and has sickle cell anemia?
Below is a pedigree chart for a family that has a history of Alkaptonuria. Individuals infected with this condition can have darkened skin, brown urine, and can suffer from joint damage and other complications. Given this pedigree answer the following questions. Given the data in the pedigree chart is this genetic condition autosomal dominant or autosomal recessive? What are the genotypes for #1, #2, and #3? If either of the 4th generation "aa" females were to mate with a homozygous dominant male would any of their offspring illustrate the phenotype? Why or why not?
Sickle cell anemia is inherited as an autosomal recessive condition. It also exhibits incomplete dominance in that the heterozygous genotype displays a mild form of the disease known as sickle cell trait while individuals with the homozygous recessive genotype have a severe form of SCA. A man who has severe sickle cell anemia marries a woman who suffers from a mild trait. What is the probabilitu they will have a child with severe SCA?What is the probability they will have a child with mild SCA? What is the probability they will have a normal child? Show ALL work using punnett squares.
Grandma Jade is affected with tuberous sclerosis, she grows benign tumors, and the trait is under control with her doctors. She is married to Grandpa Phil, who does not have the trait. Out of their four children, only one, Michael, has tuberous sclerosis. Complete the Punnett Square and indicate their genotypes.
Using the pedigree chart attached: Above is a pedigree for colorblindness. Based on the pedigree, is the disease dominant or recessive and is it sex-linked or autosomal? Why? Furthermore, what is the probability that 18 on this chart is affected but the condition, and what is the probability that 18 is a carrier? Why? Are the probability of being a carrier and an affected individual different? Why?
A typical pedigree for a family that carries neurofibromatosis is shown below. Note that carriers are not indicated with half-colored shapes in this chart. Use the letter "N" to indicate the dominant neurofibromatosis allele, and the letter "n" for the normal allele. Use the below pedigree chart and your knowledge on how to interpret a pedigree chart to answer questions # 7-9. 1 Nn nn nn 3 nn 7. Is individual #1 most likely homozygous dominant or heterozygous? Explain how you can tell. 8. What is the genotype of individual #2? Explain how you can tell. 9. What is the genotype of individual #3? Explain how you can tell. 2)
Porphyria is a genetic disorder caused by the inability to properly metabolize a component of hemoglobin. King George III is suspected to have been afflicted with this disorder. Assume that both George and his Queen suffered from this disorder and they had one afflicted child and one normal child. Is porphyria inherited in a dominant or recessive fashion? What must be the genotype of both George and his Queen? Using punnett square, show ALL work used to achieve your answer.
Neurofibromatosis-1 (NF1) is an autosomal dominant disorder where tumours form in the base layer of the skin or in nerve tissues. What is the probability that individuals II-1 and II-2 will have a genetic son with NF1? Find the image attached.
Hemophilia is a recessive sex-linked disorder (Xh). A man with hemophilia and a female carrier are concerned about their daughter inheriting the disorder. Fill in the Punnett square below by determining the gene combinations for squares 1-4. Based on your Punnett square, explain to these parents the probability (percent chance) that their daughter could have the disorder. XH X" X" Y 1 3 2 4
The father of two children is type O+, and the mother is type A+. The children are O- and A+. Given this information, what are the genotypes of the father vs. the mother at both the “I” and “Rh” alleles? Explain your rationale.