Assuming that no mitochondrial mutations occurred within the part of *her family shown on this pedigree, which of her relatives marked by the letters A-E below will have the same mitochondrial DNA sequence? (select all that apply)
her father (A)
her uncle (B)
her brother (C)
one of her female cousins (D)
one of her male cousins (E)
Explain the answers
Homework Answers
According to this pedigree
Given A= father (who is from a different family)
Also E= one of the male cousin ( whose father is also from different family)
Hence the DNA if E can match
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Assuming that no mitochondrial mutations occurred within the
part of *her family shown on this pedigree,...
Creating a pedigree chart from a family history and hypothesizing pattern of inheritance A family with...
Creating a pedigree chart from a family history and hypothesizing pattern of inheritance A family with a new disease caused by a mutant gene has been found. The family history has been collected and recorded. You will now create a pedigree chart from their family history and use the pedigree to predict the pattern of inheritance the disease follows. • Read the following family history: Patient 1 and Patient 2 visited a genetics counselor and provided their family histories. As...
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Creating a pedigree chart from a family history and hypothesizing pattern of inheritance A family with a new disease caused by a mutant gene has been found. The family history has been collected and recorded. You will now create a pedigree chart from their family history and use the pedigree to predict the pattern of inheritance the disease follows. • Read the following family history: Patient 1 and Patient 2 visited a genetics counselor and provided their family histories. As...
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Information Flag question Information text You are consulting with a family where sometimes a mutation that...
Information
Flag question
Information text
You are consulting with a family where sometimes a mutation that
leads to deafness (D) and a mutation that predisposes
individuals to early heart failure (H) are
linked. Normally these two traits sort independently
but, in some individuals, a reciprocal translocation has moved them
to the same chromosome. The chromosome maps for an individual with
two normal chromosome pairs (Normal Arrangement), and a
translocation heterozygote (Translocation Arrangement) are shown
below.
Deafness and early heart failure are...
How to do 23? 50 map units 5 map units Linkage groups d. 92 ty results...
How to do
23?
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How to do 21 and 23? 50 map units 5 map units Linkage groups d. 92...
How to do 21 and 23?
50 map units 5 map units Linkage groups d. 92 ty results from a rare, sex-limited nal puberty (P) and is expressed brother Jack and his sister Beth 10 and 14. Although Bill's mother uncles (his mother's brothers) underwent normal puberty. aploid sets of e nucleolar organizers for numbers 17-20 below) Male-limited precocious puberty results autosomal allele (P) that is dominant over the allele for normal pube only in males. Bill undergoes precocious puberty,...
Creating a pedigree chart from a family history and hypothesizing pattern of inheritance A family with a new disease caused by a mutant gene has been found. The family history has been collected and recorded. You will now create a pedigree chart from their family history and use the pedigree to predict the pattern of inheritance the disease follows. • Read the following family history: Patient 1 and Patient 2 visited a genetics counselor and provided their family histories. As...
Styles 6. Insert a picture of your pedigree chart for this family with genotypes filled in here. 7. Which pattern of inheritance do you think the disease shows? Explain your reasoning. 8. Patient 1 and Patient 2 in the pedigree chart would like to know what the chances are that they will have a child with the disease. What do you tell them? Use a Punnett Square to show your work. Using Punnett Squares for human conditions and diseases The...
Creating a pedigree chart from a family history and hypothesizing pattern of inheritance A family with a new disease caused by a mutant gene has been found. The family history has been collected and recorded. You will now create a pedigree chart from their family history and use the pedigree to predict the pattern of inheritance the disease follows. • Read the following family history: Patient 1 and Patient 2 visited a genetics counselor and provided their family histories. As...
2 3 Question 10 (5 points) Consider mitochondrial inheritance in the family shown below. (No one is shaded-in because we are not following any particular trait of interest, just mitochondrial inheritance.) 5 6 8 9 -- H Questions 1 and 2 are to be answered in order in the respective boxes below. Final answers must be entered online. Question 1: How many other people in this pedigree should have the same mitochondrial DNA as individual II-4 (not including individual II-4)?...
Q5.28. Imagine two wolves, a sister and her full-sibling brother, are working together to raise the sister's litter of 10 pups, fathered by an unrelated male. The brother could strike out on his own, in which case he would father 7 pups. However, if he leaves, only 5 pups of his sister's brood will survive. Given that Hamilton's rule says a helping behavior is favored if rB-C>0, what should the brother do to maximize his fitness? (Hint: Click here to...
U IS MOST COMMOT a population as a Select from the terms below to answer questions #17-22. One term is not used. R) Genomic imprinting S) Methylation T) Sex-influenced inheritance U) Maternal inheritance V) Sex-limited inheritance W) Complementation X) X-linked inheritance 17) Pattern baldness is controlled by two alleles: B, b. Females are bald if they are homozygous (BB) but males only need one allele B to be bald. This trait is an example of 18) A mother passes on...
Information
Flag question
Information text
You are consulting with a family where sometimes a mutation that
leads to deafness (D) and a mutation that predisposes
individuals to early heart failure (H) are
linked. Normally these two traits sort independently
but, in some individuals, a reciprocal translocation has moved them
to the same chromosome. The chromosome maps for an individual with
two normal chromosome pairs (Normal Arrangement), and a
translocation heterozygote (Translocation Arrangement) are shown
below.
Deafness and early heart failure are...
How to do
23?
50 map units 5 map units Linkage groups d. 92 ty results from a rare, sex-limited nal puberty (P) and is expressed brother Jack and his sister Beth 10 and 14. Although Bill's mother uncles (his mother's brothers) underwent normal puberty. aploid sets of e nucleolar organizers for numbers 17-20 below) Male-limited precocious puberty results autosomal allele (P) that is dominant over the allele for normal pube only in males. Bill undergoes precocious puberty, but his...
How to do 21 and 23?
50 map units 5 map units Linkage groups d. 92 ty results from a rare, sex-limited nal puberty (P) and is expressed brother Jack and his sister Beth 10 and 14. Although Bill's mother uncles (his mother's brothers) underwent normal puberty. aploid sets of e nucleolar organizers for numbers 17-20 below) Male-limited precocious puberty results autosomal allele (P) that is dominant over the allele for normal pube only in males. Bill undergoes precocious puberty,...
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