Homework Answers
The probability that their next child affected is 1 in 2 as the disorder is autosomal dominant which means altered copy of one gene is sufficient to cause disease. Considerinf father with disease and normal mother, their every child has 50% risk of getting disease. So option b seems correct and option c n d are incorrect.
option a seems incorrect because in autosomal dominant inheritance their will b no carrier
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Question 25 1 pts Achondroplasia shows autosomal dominant inheritance with complete penetrance. A man with achondroplasia...
Inheritance for Huntington's disease, an autosomal dominant traitis illustrated in the page Note - The disease...
Inheritance for Huntington's disease, an autosomal dominant traitis illustrated in the page Note - The disease allele is not lethal in the homozygous state. d. .18 "T rườởERO" HÀ THỜ dood. " (4pts) Which mating clearly demonstrates autosomal dominant inheritance and excludes all other patterns? Explain. The mating between 111.15,16 because we have two parents that are affected with Huntingtons dobesa disease and they Produce an ort Spring with noorrect of the diesease. (pts) Identify the genotypes of the following...
In general, the following characteristics suggest (but do not prove) specific inheritance patterns: Autosomal recessive inheritance:...
In general, the following characteristics suggest (but do not prove) specific inheritance patterns: Autosomal recessive inheritance: -affected individuals can be born to unaffected parents -if both parents are affected, all children are affected -observable effect of relatedness (consanguinity) -horizontal" inheritance: trait appears at once among several members of one generation (siblings) *** Autosomal dominant inheritance each affected individual has an affected parent -when one parent is affected, transmission to the offspring (on average) *** -two unaffected parents do not transmit...
2. Achondroplasia is a short-limbed dwarfism that is inherited as an autosomal dominant disease. The mutant...
2. Achondroplasia is a short-limbed dwarfism that is inherited as an autosomal dominant disease. The mutant allele that causes this form of dwarfism (D) is dominant to the normal allele at this location (d). Individuals who inherit 2 alleles for dwarfism (DD) typically have a very severe form of achondroplasia that causes extreme shortening of the bones and an underdeveloped rib cage. These individuals are usually miscarried or stillborn. Tom and Vonna both have achondroplasia (but each of them has...
6 A human trait that is caused by an autosomal dominant mutant allele has a penetrance...
6
A human trait that is caused by an autosomal dominant mutant allele has a penetrance of 50%. A man who is heterozygous for this mutant allele marries a woman who is homozygous recessive for the normal allele. If they have two children then what is the probability that both children will show the normal phenotype? O 1/4 o 1/2 03/16 0 7/8 09/16
Look carefully at the pedigrees below and: 1) indicate whether the transmission appears autosomal or sex-linked...
Look carefully at the pedigrees below and:
1) indicate whether the transmission appears autosomal or
sex-linked
2) indicate whether the transmission appears dominant or
recessive
3) provide at least two characteristics for each that support
your conclusion.
In general, the following characteristics suggest (but do not prove) specific inheritance patterns: Autosomal recessive inheritance: -affected individuals can be born to unaffected parents -if both parents are affected, all children are affected -observable effect of relatedness (consanguinity) -horizontal" inheritance: trait appears at...
1. (2 pts) Attached ear lobes (f) are inherited as an autosomal recessive trait. The dominant...
1. (2 pts) Attached ear lobes (f) are inherited as an autosomal recessive trait. The dominant allele, F, produces free hanging ear lobes. Sam and Beth both have free earlobes, but their first child has attached earlobes. a. What are the likely genotypes of Sam and Beth with respect to the ear lobe locus? Sam: F Beth: FF b. With respect to the earlobe locus, Sam's genotype is homozygous,/(heterozygous or hemizygous? (Circle the correct answer). c. If Sam and Beth...
a. Determine the most probable mode of inheritance: autosomal or sex-linked, dominant or recessive, of the...
a. Determine the most probable mode of inheritance: autosomal or sex-linked, dominant or recessive, of the disorders in the two pedigrees shown below and indicate the genotypes of as many individuals as possible. 0 0 | ●ㅇ 이 vod 0d b. If individual IV-1 from the first pedigree marries an affected woman, what is the probability that their first child is affected by the disorder? c. If individual IV-3 from the second pedigree marries a normal man, what is the...
1a. A boy has Duchenne muscular dystrophy, an X-linked recessive trait. His maternal uncle had died...
1a. A boy has Duchenne muscular dystrophy, an X-linked recessive trait. His maternal uncle had died of muscular dystrophy at the age of 21 years. What is the probability that this child's siblings will be affected? i. It depends whether his mother is a carrier or not ii. 50% iii. 25% iv. 75% v. 0% 1b. Neurofibromatosis type 1 is one of the most common autosomal dominant disorders. A woman with neurofibromatosis type 1 has an unaffected partner. Which of...
QUESTION 3 If the characteristic depicted in the pedigree below is subject to complete penetrance, which...
QUESTION 3 If the characteristic depicted in the pedigree below is subject to complete penetrance, which of the following modes of inheritance are possible? 3 4 1 2 Y linked Mitochondrial X linked recessive Autosomal recessive QUESTION 4 5 p. If the characteristic depicted in the pedigree below is subject to complete penetrance, what is the genotype of individual II-3? 2 2 3 Shop N 1 2 3 AA, homozygous dominant aa, homozygous recessive Aa, heterozygous QUESTION 5 If the...
Follow-Up Questions 1. Your brother has an autosomal recessive disorder, while you are unaffected. Neither one...
Follow-Up Questions 1. Your brother has an autosomal recessive disorder, while you are unaffected. Neither one of your parents is affected. Explain how this is possible. 2. Using the above situation, what is the probability that you carry the recessive allele? 3. A couple wants to have a child, but the mother has a brother who is affected by cystic fibrosis. They seek out the advice of a genetic counselor at their local hospital to determine what, if any, chance...
Inheritance for Huntington's disease, an autosomal dominant traitis illustrated in the page Note - The disease allele is not lethal in the homozygous state. d. .18 "T rườởERO" HÀ THỜ dood. " (4pts) Which mating clearly demonstrates autosomal dominant inheritance and excludes all other patterns? Explain. The mating between 111.15,16 because we have two parents that are affected with Huntingtons dobesa disease and they Produce an ort Spring with noorrect of the diesease. (pts) Identify the genotypes of the following...
In general, the following characteristics suggest (but do not prove) specific inheritance patterns: Autosomal recessive inheritance: -affected individuals can be born to unaffected parents -if both parents are affected, all children are affected -observable effect of relatedness (consanguinity) -horizontal" inheritance: trait appears at once among several members of one generation (siblings) *** Autosomal dominant inheritance each affected individual has an affected parent -when one parent is affected, transmission to the offspring (on average) *** -two unaffected parents do not transmit...
6
A human trait that is caused by an autosomal dominant mutant allele has a penetrance of 50%. A man who is heterozygous for this mutant allele marries a woman who is homozygous recessive for the normal allele. If they have two children then what is the probability that both children will show the normal phenotype? O 1/4 o 1/2 03/16 0 7/8 09/16
Look carefully at the pedigrees below and:
1) indicate whether the transmission appears autosomal or
sex-linked
2) indicate whether the transmission appears dominant or
recessive
3) provide at least two characteristics for each that support
your conclusion.
In general, the following characteristics suggest (but do not prove) specific inheritance patterns: Autosomal recessive inheritance: -affected individuals can be born to unaffected parents -if both parents are affected, all children are affected -observable effect of relatedness (consanguinity) -horizontal" inheritance: trait appears at...
1. (2 pts) Attached ear lobes (f) are inherited as an autosomal recessive trait. The dominant allele, F, produces free hanging ear lobes. Sam and Beth both have free earlobes, but their first child has attached earlobes. a. What are the likely genotypes of Sam and Beth with respect to the ear lobe locus? Sam: F Beth: FF b. With respect to the earlobe locus, Sam's genotype is homozygous,/(heterozygous or hemizygous? (Circle the correct answer). c. If Sam and Beth...
a. Determine the most probable mode of inheritance: autosomal or sex-linked, dominant or recessive, of the disorders in the two pedigrees shown below and indicate the genotypes of as many individuals as possible. 0 0 | ●ㅇ 이 vod 0d b. If individual IV-1 from the first pedigree marries an affected woman, what is the probability that their first child is affected by the disorder? c. If individual IV-3 from the second pedigree marries a normal man, what is the...
QUESTION 3 If the characteristic depicted in the pedigree below is subject to complete penetrance, which of the following modes of inheritance are possible? 3 4 1 2 Y linked Mitochondrial X linked recessive Autosomal recessive QUESTION 4 5 p. If the characteristic depicted in the pedigree below is subject to complete penetrance, what is the genotype of individual II-3? 2 2 3 Shop N 1 2 3 AA, homozygous dominant aa, homozygous recessive Aa, heterozygous QUESTION 5 If the...
Follow-Up Questions 1. Your brother has an autosomal recessive disorder, while you are unaffected. Neither one of your parents is affected. Explain how this is possible. 2. Using the above situation, what is the probability that you carry the recessive allele? 3. A couple wants to have a child, but the mother has a brother who is affected by cystic fibrosis. They seek out the advice of a genetic counselor at their local hospital to determine what, if any, chance...
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