Given the pedigree below for a rare autosomal trait, what is the likelihood that Persons A and B would have an affected child?
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Given the pedigree below for a rare autosomal trait, what is the
likelihood that Persons A...
A pedigree affected by a rare human autosomal recessive trait is shown below. ODO What is...
A pedigree affected by a rare human autosomal recessive trait is shown below. ODO What is the probability that III-2 is a carrier? (enter your answer as a percentage; if the answer is 83% enter 83) Answer:
please show work 4. The pedigree shown at below is for a rare autosomal recessive trait....
please show work
4. The pedigree shown at below is for a rare autosomal recessive trait. What is the probability that individual 1.2 was heterozygous for this trait? a. 1 b. 1/2 c. 1/4 d. 0 e. cannot determine
Alkaptonuria (AKU) is a disorder that causes defects in metabolism of the amino acids phenylalani...
A)
B)
Alkaptonuria (AKU) is a disorder that causes defects in metabolism of the amino acids phenylalanine and tyrosine, leading to a variety of symptoms (e.g. urine is black). AKU is a rare autosomal recessive disease. Based on the pedigree below, if persons A and B mate, what is the probability that their first child will have AKU? a. 1/48 c. 1/64 e. none of the above b. 1/96 Alkaptonuria (AKU) Is a rare autosomal disorder that causes defects in...
93. The pedigree below shows the sex-linked recessive inheritance of Nance-Horan syndrome, a rare Mendelian disorder...
93. The pedigree below shows the sex-linked recessive inheritance of Nance-Horan syndrome, a rare Mendelian disorder in which affected persons have cataracts and abnormally shaped teeth. What is the probability that the first child of IV-6 and V-3 would have Nance-Horan syndrome? Iv A) 114 B) 1/2 C) 1/8 D) 3/16 E) 3/4
11. A rare autosomal dominant condition affects the following family pedigree
11. A rare autosomal dominant condition affects the following family pedigree. What is the probability that the unborn child marked with the question mark is affected by the condition? Express the answer as a decimal fraction with two digits after the decimal point. Do not round the fraction. (.e 1/3 = 0.27) 12. Which of the following is not a necessary step in lytic bacteriophage infection cycle? Select one: a. Injection of the viral genome b. Viral protein is synthesized by the host cell c. The...
this is all that im given Question 3: (4 points) Consider the following pedigree: O O...
this is all that im given
Question 3: (4 points) Consider the following pedigree: O O 1 2 3 4 5 Characterize each of the following modes of inheritance as: Impossible, Possible, or Most likely. Justify your answers. a. Autosomal dominant b. Autosomal recessive X-linked dominant d. X-linked recessive e. Y-linked f. Going with the most likely mode of inheritance .... Assume individual V-1 marries a phenotypically normal male. What is the likelihood that their first child is affected with...
A rare autosomal dominant condition affects the following family pedigree. What is the probability that the...
A rare autosomal dominant condition affects the following family pedigree. What is the probability that the unborn child marked with the question mark is affected by the condition? Express the answer as a decimal fraction with two digits after the decimal point. Do not round the fraction. (i.e 1/3 = 0.33) Answer:
The following pedigree corresponds to a family affected by a rare autosomal recessive condition. What is...
The following pedigree corresponds to a family affected by a rare autosomal recessive condition. What is the probability for the unborn child marked with "?"to be a carrier? Provide your answer as a decimal fraction up to the second digit after the period and do not round up or down. (i.e. if your result is 1/3 then write 0.33) 02 ? Answer:
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...
Alkaptonuria (AKU) is a rare autosomal disorder that causes defects in metabolism of the amino acids...
Alkaptonuria (AKU) is a rare autosomal disorder that causes
defects in metabolism of the amino acids phenylalanine and
tyrosine. Based on the pedigree below, what is the chance that
individual IV-1 will display this trait?
a. 1/16 b. 1/12 c. 1/24 d. 1/18 e. 1/8
명문
A pedigree affected by a rare human autosomal recessive trait is shown below. ODO What is the probability that III-2 is a carrier? (enter your answer as a percentage; if the answer is 83% enter 83) Answer:
please show work
4. The pedigree shown at below is for a rare autosomal recessive trait. What is the probability that individual 1.2 was heterozygous for this trait? a. 1 b. 1/2 c. 1/4 d. 0 e. cannot determine
A)
B)
Alkaptonuria (AKU) is a disorder that causes defects in metabolism of the amino acids phenylalanine and tyrosine, leading to a variety of symptoms (e.g. urine is black). AKU is a rare autosomal recessive disease. Based on the pedigree below, if persons A and B mate, what is the probability that their first child will have AKU? a. 1/48 c. 1/64 e. none of the above b. 1/96 Alkaptonuria (AKU) Is a rare autosomal disorder that causes defects in...
93. The pedigree below shows the sex-linked recessive inheritance of Nance-Horan syndrome, a rare Mendelian disorder in which affected persons have cataracts and abnormally shaped teeth. What is the probability that the first child of IV-6 and V-3 would have Nance-Horan syndrome? Iv A) 114 B) 1/2 C) 1/8 D) 3/16 E) 3/4
this is all that im given
Question 3: (4 points) Consider the following pedigree: O O 1 2 3 4 5 Characterize each of the following modes of inheritance as: Impossible, Possible, or Most likely. Justify your answers. a. Autosomal dominant b. Autosomal recessive X-linked dominant d. X-linked recessive e. Y-linked f. Going with the most likely mode of inheritance .... Assume individual V-1 marries a phenotypically normal male. What is the likelihood that their first child is affected with...
A rare autosomal dominant condition affects the following family pedigree. What is the probability that the unborn child marked with the question mark is affected by the condition? Express the answer as a decimal fraction with two digits after the decimal point. Do not round the fraction. (i.e 1/3 = 0.33) Answer:
The following pedigree corresponds to a family affected by a rare autosomal recessive condition. What is the probability for the unborn child marked with "?"to be a carrier? Provide your answer as a decimal fraction up to the second digit after the period and do not round up or down. (i.e. if your result is 1/3 then write 0.33) 02 ? Answer:
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...
Alkaptonuria (AKU) is a rare autosomal disorder that causes
defects in metabolism of the amino acids phenylalanine and
tyrosine. Based on the pedigree below, what is the chance that
individual IV-1 will display this trait?
a. 1/16 b. 1/12 c. 1/24 d. 1/18 e. 1/8
명문
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