Homework Answers
Chances of v3 being carrier 1/2 and IV 6 is normal
They carrir mother having affected child is 1/4
This child being affected by this syndrome is 14x1/2= 1/8
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93. The pedigree below shows the sex-linked recessive inheritance of Nance-Horan syndrome, a rare Mendelian disorder...
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...
The pedigree below shows the inheritance of a rare mutant phenotype in humans, congenital cataracts. If...
The pedigree below shows the inheritance of a rare mutant
phenotype in humans, congenital cataracts. If we use the letter E
to represent the alleles for this disorder, what are the possible
genotypes for person A?
ーーーーー -O C Y e YYX Ee eE A EEeXXX NOOOO B
The pedigree shows the occurrence of a X linked recessive mendelian disease in a human family....
The pedigree shows the occurrence of a X linked recessive mendelian disease in a human family. Two unaffected family members were genotyped at a microsatellite locus and two different microsatellite alleles were observed (M1 and M2) I M1/M1 II 1 M1 M2 III 3 IV 3 5 a) Assume the disease and the microsatellite locus are completely linked. What is the genotype of individual IV-4 (give both disease and micrsatellite alleles in the genotype)? b) Assume that the disease locus...
10. In humans Wiskott–Aldrich syndrome (WAS) is a rare sex-linked recessive disease characterized by eczema, thrombocytopenia...
10. In humans Wiskott–Aldrich syndrome (WAS) is a rare sex-linked recessive disease characterized by eczema, thrombocytopenia (low platelet count), immune deficiency, and bloody diarrhea. This disease is due to a sex-linked recessive allele. a. Examine the statement below. Is this statement true or false? Why? Explain. Boys usually inherit sex-linked recessive disorders from their fathers. Sarah is healthy and but her brother has WAS. Her mother and father both have healthy phenotypes. Sarah marries Fred, a healthy man without WAS....
Part B - Identify the mode of inheritance Look over the pedigree you constructed in Part...
Part B - Identify the mode of inheritance Look over the pedigree you constructed in Part A. Based on the inheritance pattern, which mode of inheritance must be the cause of galactosemia? Based on the inheritance pattern, which mode of inheritance must be the cause of galactosemia? sex-linked dominant autosomal dominant sex-linked recessive autosomal recessive SubmitHintsMy AnswersGive UpReview Part Part C - Predicting the probability of inheritance Jane and John are considering having another child. Given the pedigree you constructed...
The mode of inheritance for the following pedigree is X-linked recessive. - O 1 2 3...
The mode of inheritance for the following pedigree is X-linked recessive. - O 1 2 3 4 5 6 N III O 1 2 3 5 6 IV 1 2 If individuals III-1 and III-2 were to have another child, what is the probability that they would express the trait? Explain your reasoning.
The pedigree below shows the inheritance pattern of a sex-linked allele for one family. What is...
The pedigree below shows the inheritance pattern of a sex-linked allele for one family. What is true about the genotype of individuall-2? 1-1 1-2 II-1 II-2 II-3 II-4 III-1 III-2 The disease is caused by a dominant allele (D) and his genotype is dd He must have the genotype X'Y The disease is caused by having two recessive alleles (dd) and his genotype is He has the recessive disease allele on his X chromosome XY He has the dominant disease...
Consider the following pedigree of a rare X-linked recessive disease. a) If individuals A and B...
Consider the following pedigree of a rare X-linked recessive disease. a) If individuals A and B have a child, what is the probability that the child will have the disease? b) If individuals C and D have a child, what is the probability that the child will have the disease? c) If the first child of C and D is normal, what is the probability that their second child will have the disease? d) If the first child of C...
The mode of inheritance for the following pedigree is X-linked recessive. If individuals III-1 and III-2...
The mode of inheritance for the following pedigree is X-linked recessive. If individuals III-1 and III-2 were to have another child, what is the probability that they would express the trait? Explain your reasoning.
모모모 < 모 2 1 | 미모 모 오 or lo III = - - genetic...
모모모 < 모 2 1 | 미모 모 오 or lo III = - - genetic disorder is segregating. 3. Each of the pedigrees shown represents a human family within which a genetic disorder is se Assume the two traits are extremely rare in the population and completely penetrant. Part 1. For the first pedigree. lisorder: autosomal recessive, autosomal a. Determine the most probable inheritance pattern of the disorder: autosomal recessive dominant, X-linked recessive or X-linked dominant. b. Indicate 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...
The pedigree below shows the inheritance of a rare mutant
phenotype in humans, congenital cataracts. If we use the letter E
to represent the alleles for this disorder, what are the possible
genotypes for person A?
ーーーーー -O C Y e YYX Ee eE A EEeXXX NOOOO B
The pedigree shows the occurrence of a X linked recessive mendelian disease in a human family. Two unaffected family members were genotyped at a microsatellite locus and two different microsatellite alleles were observed (M1 and M2) I M1/M1 II 1 M1 M2 III 3 IV 3 5 a) Assume the disease and the microsatellite locus are completely linked. What is the genotype of individual IV-4 (give both disease and micrsatellite alleles in the genotype)? b) Assume that the disease locus...
The mode of inheritance for the following pedigree is X-linked recessive. - O 1 2 3 4 5 6 N III O 1 2 3 5 6 IV 1 2 If individuals III-1 and III-2 were to have another child, what is the probability that they would express the trait? Explain your reasoning.
The pedigree below shows the inheritance pattern of a sex-linked allele for one family. What is true about the genotype of individuall-2? 1-1 1-2 II-1 II-2 II-3 II-4 III-1 III-2 The disease is caused by a dominant allele (D) and his genotype is dd He must have the genotype X'Y The disease is caused by having two recessive alleles (dd) and his genotype is He has the recessive disease allele on his X chromosome XY He has the dominant disease...
Consider the following pedigree of a rare X-linked recessive disease. a) If individuals A and B have a child, what is the probability that the child will have the disease? b) If individuals C and D have a child, what is the probability that the child will have the disease? c) If the first child of C and D is normal, what is the probability that their second child will have the disease? d) If the first child of C...
모모모 < 모 2 1 | 미모 모 오 or lo III = - - genetic disorder is segregating. 3. Each of the pedigrees shown represents a human family within which a genetic disorder is se Assume the two traits are extremely rare in the population and completely penetrant. Part 1. For the first pedigree. lisorder: autosomal recessive, autosomal a. Determine the most probable inheritance pattern of the disorder: autosomal recessive dominant, X-linked recessive or X-linked dominant. b. Indicate the...
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