d The pedigree above shows inheritance of an X-linked recessive disorder. Use this pedigree to answer questions X-Y below. 22) If individual II-2 marries an unaffected male, what are the chances they will have an affected son? a) 1/2 b) 1/4 c) 1/6 d) 1/8 e) 0 23) In generation III, how many individuals' genotypes are known for certain? a) 5 b) 3 c) 4 d) 2 e) 0

d The pedigree above shows inheritance of an X-linked recessive disorder. Use this pedigree to answer questions X-Y below. 22) If individual II-2 marries an unaffected male, what are the chances they will have an affected son? a) 1/2 b) 1/4 c) 1/6 d) 1/8 e) 0 23) In generation III, how many individuals' genotypes are known for certain? a) 5 b) 3 c) 4 d) 2 e) 0

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Description: Please answer both questions in detail. Correct answers are highlighted. ㅁㅁㅇㅁ ㅎㅁ이The pedigree above shows inheritance of an X-linked recessive disorder. Use this pedigree to answerquestions X-Y below.22) If individual II-2 marries an unaffected male,

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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Now assume that the pedigree shown in question 1 shows the inheritance of a rare genetic disease. a) The disease is most likely autosomal dominant b) The disease is most likely autosomal recessive c) The disease is equally likely to be either autosomal dominant or autosomal recessive, but cannot be x-linked d) Cannot be determined from the information given
Shown below is a pedigree for Phenylketonuria (PKU), an autosomal recessive metabolic disorder. The characteristic feature of PKU is severe mental retardation A) What is the probability that individual II-1 is heterozygous for this gene? B) What is the probability that individual III-4 is heterozygous for this gene? C) If individuals III-3 and III-4 were to marry, what is the probability that their child would express PKU?
Below is a pedigree of a human genetic disease in which solid color indicates affected individuals. Assume that the disease is caused by a gene that can have the alleles A or a. a) Based on this pedigree, what is the most likely mode of inheritance? b) What is/are the possible genotype/s of person 1? c) What is/are the possible genotype (s) of person 4 ? Explain your answers.
PKU is an inherited disease caused by a recessive allele. If a woman and her husband, who are both carriers (heterozygotes) for the disorder, have three children, what is the probability of each of the following? a) All three children are of normal phenotype. b) All three children have the disease. c) Any 2 of the three children have the normal phenotype.
In humans, cystic fibrosis is a disease caused by a recessive allele (). Individuals with normal (wildtype) phenotype have the genotype (F). If two heterozygous individuals marry and have 8 children, what is the probability that: a) four will be normal and four will have cystic fibrosis? b) one will have cystic fibrosis and seven will be normal? c) All eight children will have cystic fibrosis?
Using the pedigree chart, explain: a) The number of generations seen. b) If all blue-coloured shapes are affected with disease X- how many males are affected? how many females are affected? c) Does this disease have a dominant or recessive inheritance pattern? Justify your answer.
This pedigree consist of cystic fibrosis that is an inherited disease caused by f a recessive allele. Find the genotypes of X and M? Given: O normal female □ normal male ◍ cystic fibrosis female ▨ cystic fibrosis male A) M= Ff X=Ff B) M=Ff X=ff C) M=ff X=ff D) M=ff X=FF
A pedigree lists a father as the proband for a genetic disorder that he inherited from his mother. Out of his 3 children, his son inherits the condition but his two daughters do not. What can you hypothesize about this disorder? a) It is an X-linked recessive disorder. b) His wife is also a carrier of an affected X-chromosome, too. c) His son had to inherit a defective X allele from his mother since he obviously received a Y from Dad. d) Although his daughters inherited the father's mutant X allele, a wt X allele from their mother prevented them from inheriting the disorder. e) All the answers could be correct.
Circle any inheritance patterns that could explain this pedigree. Assume individuals marrying into the family do not have a mutant allele. Please refer to the image attached. A) Paternally imprinted B) Maternally imprinted C) Maternal inheritance D) Autosomal recessive E) Autosomal dominant F) X-linked recessive G) X-linked dominant
Albinism in humans is inherited as a simple recessive trait.Determine the genotypes of the parents and offspring for the following families. When two alternative genotypes are possible,list both.(a) Two parents without albinism have five children, four withoutalbinism and one with albinism.(b) A male without albinism and a female with albinism havesix children, all without albinism.
In humans, the allele for red-green color blindness is X-linked and recessive. An XY man with normal color vision marries a color-blind XX woman who gives birth to a XX color-blind daughter. A] What is the phenotype and genotype ratios possible for a child born to this couple. B] What is the probability that the second XX daughter of this same couple will also be color blind? C] What is the probability that the next child this couple produces together will be a color-blind XY son? D] What can you tell me about the first color-blind daughter born?
The pedigree shows a family in which several members have suffered from one and the same disease (look at the picture to be able to answer) a) Is it a dominant or recessive allele that causes the disease? Motivate your answer. b) Is allele autosomal or sex-linked? Motivate your answer. c) What is the probability that III-3 and III-4 will have a healthy child? Motivate your answer.