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ANSWER :
X-linked recessive genetic disorder (e.g.- colour blindness) is phenotypically appear when all the X-chromosomes present in the individuals have affected allele. All the female individuals, who have affected allele on their one X-chromosome are called as disease carriers, it doesn't affect by disease itself but can transfer affected allele to male individuals of next generation and caused them ill. Hence the shown pedigree chart most suitably represent the X-linked recessive disorder.
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00 ood. God Teens OV 926 okoladi 10. Assuming complete penetrance, the most likely genetic mechanism...
QUESTION 12 10 points Save Answer What is the likely mode of inheritance for the genetic...
QUESTION 12 10 points Save Answer What is the likely mode of inheritance for the genetic disorder shown in the pedigree below? MItochondrial Autosomal recessive X-linked recessive X-linked dominant
1) Select the true statements about dominant and recessive genes, assuming complete penetrance of the genotype....
1) Select the true statements about dominant and recessive genes, assuming complete penetrance of the genotype. Circle all that apply. (1.5) For an offspring to be phenotypically dominant for a trait, at least one parent will show the trait. For an offspring to be phenotypically recessive for a trait, at least one parent will show the trait. In incomplete dominant or codominant traits, heterozygotes will have a different phenotype than either homozygote. If both parents show a recessive trait, then...
(a) For each pedigree, indicate the most likely mode of inheritance (6 pts) (2 pts) (b)...
(a) For each pedigree, indicate the most likely mode of inheritance (6 pts) (2 pts) (b) In pedigree B, circle all individuals who are heterozygous. or to 0 0 - 이 SSO | 호 co | or - TTT Choices: A. Y-linked, B. X-linked dominant C. recessive, D. Autosomal dominant, E. Autosomal recessive.
(a) For each pedigree, indicate the most likely mode of inheritance (6 pts) B. (b) In...
(a) For each pedigree, indicate the most likely mode of inheritance (6 pts) B. (b) In pedigree B, circle all individuals who are heterozygous. (2 pts) OG 0 0 0 0 0 호 c GO GO CD p. | 8 日 ITE | ODDC D Choices: A. Y-linked, B. X-linked dominant C. recessive, D. Autosomal dominant, E. Autosomal recessive.
Question 3 The following human pedigree shows a family affected by a specific disease. Assume that...
Question 3 The following human pedigree shows a family affected by a specific disease. Assume that the individuals marked with an asterisk () do not carry any allele associated with the affected phenotype and that no other mutation spontaneously occurs. Also assume complete penetrance a) State the most likely mode of inheritance for this disease. Choose from: autosomal dominant, autosomal recessive, X-linked dominant, X-linked recessive b) Write all possible genotypes of the following individuals in the pedigree. Use the uppercase...
QUESTION 9 5 pe If the characteristic depicted in the pedigree below is rare and subject...
QUESTION 9 5 pe If the characteristic depicted in the pedigree below is rare and subject to complete penetrance, it is likely to be X-linked recessive? 5 6 7 -OOO No, because individuals ll-2 and 11-4 are not affected No, because individuals 111-4 and III-6 are not affected Yes, because individuals III-4 and III-6 are not affected Yes, because only females are affected in generation 11 1. The gene for cystic fibrosis (normal dominant allele CF and abnormal recessive allele...
7. What type of trait is found the most often in nature? a. mutant trait b....
7. What type of trait is found the most often in nature? a. mutant trait b. wild-type trait C. dominant trait d. recessive trait 8. A heterozygous person that has one disease allele and one normal allele is referred to as a 9. Tay-Sachs is an autosomal recessive disease. A couple (Jack and Jill) is worried about having a child who has Tay-Sachs, because Jack had a brother with the deadly disease. Since they wanted to have children, they sought...
need help with these questions please. 12: In the F2 generation of Mendel's monohybrid cross, the...
need help with these questions please.
12: In the F2 generation of Mendel's monohybrid cross, the two heterozygous parent corn plants (Pp x Pp) produced offspring with the following genotypes e) PP (purple). Pp (purple). Pp(white). f) All purple g) All White h) All pink 15: A female fruit fly that is homozygous for white mutation will have the genotype a) W-w- b) Wºw c) W/W- d) W/Y 21: A father is heterozygous for the ability to roll the tongue....
Circle the correct answer, there may be more than one correct answer 1. Diploid Organisms: a)...
Circle the correct answer, there may be more than one correct answer 1. Diploid Organisms: a) typically have 23 pairs of chromosomes b) are heterozygous for a trait when they carry different alleles c) carry 2 copies of chromosomes d) are homozygous for a trait when they carry different alleles 2. Why are garden peas a good subject for Mendel's experiments? a) garden peas had either or traits b) garden pess could self-pollinate to produce offspring of the same variety...
7. Tra diploid organism has the genotype AABh, what% of its gametes would you expect to...
7. Tra diploid organism has the genotype AABh, what% of its gametes would you expect to have the genotype A (assume that A/a locus and B/blocus are found on different chromosomes)? a) 1598 b) 2596 c) 5096 d) 7546 8. Phenylketonuria is an inherited human genetic disorder resulting from a mutation to the PAH gene. Individuals with mutant forms of the PAW gene exhibit leaming deficits, abnormal skin pigmentation, as well as heart problems. This is an example of: a)...
QUESTION 12 10 points Save Answer What is the likely mode of inheritance for the genetic disorder shown in the pedigree below? MItochondrial Autosomal recessive X-linked recessive X-linked dominant
(a) For each pedigree, indicate the most likely mode of inheritance (6 pts) (2 pts) (b) In pedigree B, circle all individuals who are heterozygous. or to 0 0 - 이 SSO | 호 co | or - TTT Choices: A. Y-linked, B. X-linked dominant C. recessive, D. Autosomal dominant, E. Autosomal recessive.
(a) For each pedigree, indicate the most likely mode of inheritance (6 pts) B. (b) In pedigree B, circle all individuals who are heterozygous. (2 pts) OG 0 0 0 0 0 호 c GO GO CD p. | 8 日 ITE | ODDC D Choices: A. Y-linked, B. X-linked dominant C. recessive, D. Autosomal dominant, E. Autosomal recessive.
Question 3 The following human pedigree shows a family affected by a specific disease. Assume that the individuals marked with an asterisk () do not carry any allele associated with the affected phenotype and that no other mutation spontaneously occurs. Also assume complete penetrance a) State the most likely mode of inheritance for this disease. Choose from: autosomal dominant, autosomal recessive, X-linked dominant, X-linked recessive b) Write all possible genotypes of the following individuals in the pedigree. Use the uppercase...
QUESTION 9 5 pe If the characteristic depicted in the pedigree below is rare and subject to complete penetrance, it is likely to be X-linked recessive? 5 6 7 -OOO No, because individuals ll-2 and 11-4 are not affected No, because individuals 111-4 and III-6 are not affected Yes, because individuals III-4 and III-6 are not affected Yes, because only females are affected in generation 11 1. The gene for cystic fibrosis (normal dominant allele CF and abnormal recessive allele...
7. What type of trait is found the most often in nature? a. mutant trait b. wild-type trait C. dominant trait d. recessive trait 8. A heterozygous person that has one disease allele and one normal allele is referred to as a 9. Tay-Sachs is an autosomal recessive disease. A couple (Jack and Jill) is worried about having a child who has Tay-Sachs, because Jack had a brother with the deadly disease. Since they wanted to have children, they sought...
need help with these questions please.
12: In the F2 generation of Mendel's monohybrid cross, the two heterozygous parent corn plants (Pp x Pp) produced offspring with the following genotypes e) PP (purple). Pp (purple). Pp(white). f) All purple g) All White h) All pink 15: A female fruit fly that is homozygous for white mutation will have the genotype a) W-w- b) Wºw c) W/W- d) W/Y 21: A father is heterozygous for the ability to roll the tongue....
Circle the correct answer, there may be more than one correct answer 1. Diploid Organisms: a) typically have 23 pairs of chromosomes b) are heterozygous for a trait when they carry different alleles c) carry 2 copies of chromosomes d) are homozygous for a trait when they carry different alleles 2. Why are garden peas a good subject for Mendel's experiments? a) garden peas had either or traits b) garden pess could self-pollinate to produce offspring of the same variety...
7. Tra diploid organism has the genotype AABh, what% of its gametes would you expect to have the genotype A (assume that A/a locus and B/blocus are found on different chromosomes)? a) 1598 b) 2596 c) 5096 d) 7546 8. Phenylketonuria is an inherited human genetic disorder resulting from a mutation to the PAH gene. Individuals with mutant forms of the PAW gene exhibit leaming deficits, abnormal skin pigmentation, as well as heart problems. This is an example of: a)...
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